A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196886



Internal ID21335682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85062032..85062089hg38UCSC Ensembl
chr6:85771750..85771807hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925146
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196886
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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