A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170479



Internal ID21465836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2632230..2632230hg38UCSC Ensembl
chrY:2500271..2500271hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605549
Supporting Variants
SamplesHG03065
Known GenesCD99P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170479
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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