A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967399



Internal ID19245517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31246023..31453823hg38UCSC Ensembl
Outerchr6:31213800..31421600hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38207801
hg19207801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112899
Supporting Variants
SamplesKWS2
Known GenesHLA-B, HLA-C, MICA, MIR6891
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967399
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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