A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697474



Internal ID21219323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3092582..3092922hg38UCSC Ensembl
chr6:3092816..3093156hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814876
Supporting Variants
Samples
Known GenesRIPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697474
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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