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nsv4903003

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,544

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 511 SVs from 36 studies. See in: genome view    
Submitted genomic22,304,226-22,369,769Question Mark
Overlapping variant regions from other studies: 512 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):24,450,373-24,515,916Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4903003Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000024.10ChrY22,304,22622,369,769
nsv4903003RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000024.9ChrY24,450,37324,515,916

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16591078deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16591078Submitted genomicNC_000024.10:g.223
04226_22369769del
GRCh38 (hg38)NC_000024.10ChrY22,304,22622,369,769
nssv16591078RemappedPerfectNC_000024.9:g.2445
0373_24515916del
GRCh37.p13First PassNC_000024.9ChrY24,450,37324,515,916

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16591078<0.0011215802
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