A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170681



Internal ID21452321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3241238..3243273hg38UCSC Ensembl
chrY:3109279..3111314hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382036
hg192036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666701
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170681
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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