A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169385



Internal ID21431178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11090292..11090419hg38UCSC Ensembl
chrY:13245968..13246095hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671265
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169385
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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