A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191950



Internal ID21330814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37128264..37128264hg38UCSC Ensembl
chr1:37593865..37593865hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941814
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191950
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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