A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170663



Internal ID21462115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:321631..321631hg38UCSC Ensembl
chrY:232366..232366hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609546
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170663
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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