A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952972



Internal ID21373041
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205274
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952972
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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