A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205274



Internal ID21344076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21670913..21670913hg38UCSC Ensembl
chrY:23832799..23832799hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952972
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205274
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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