A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187860



Internal ID21326695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892616..84892616hg38UCSC Ensembl
chr2:85119740..85119740hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945642
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187860
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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