A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170639



Internal ID21488107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2773505..2773505hg38UCSC Ensembl
chrY:2641546..2641546hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612272
Supporting Variants
SamplesNA18534
Known GenesXGPY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170639
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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