A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189182



Internal ID21327984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206782064..206782064hg38UCSC Ensembl
chr1:206955409..206955409hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950944
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189182
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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