A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696542



Internal ID21218396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150372380..150372505hg38UCSC Ensembl
chr6:150693516..150693641hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812354
Supporting Variants
Samples
Known GenesIYD
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696542
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.625


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