A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170998



Internal ID21508006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56697030..56697159hg38UCSC Ensembl
chrY:58893712..58893841hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666716
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170998
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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