A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15197310



Internal ID21336106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54915508..54915836hg38UCSC Ensembl
chr6:54780306..54780634hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947829
Supporting Variants
SamplesHG002
Known GenesFAM83B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15197310
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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