A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170575



Internal ID21487559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5004801..5004890hg38UCSC Ensembl
chrY:4872842..4872931hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666001
Supporting Variants
SamplesNA18534
Known GenesPCDH11Y
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170575
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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