A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202628



Internal ID21341432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150589727..150589727hg38UCSC Ensembl
chr6:150910863..150910863hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951067
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202628
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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