A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955613



Internal ID19216517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:116429659..116429968hg38UCSC Ensembl
Outerchr6:116750822..116751131hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116825
Supporting Variants
SamplesKWS1
Known GenesDSE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955613
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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