A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169949



Internal ID21480206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1681966..1681966hg38UCSC Ensembl
chrY:1750859..1750859hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624380
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169949
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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