A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975015



Internal ID19245173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:55443008..55443144hg38UCSC Ensembl
Outerchr6:55307806..55307942hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137081
Supporting Variants
SamplesKWS2
Known GenesHMGCLL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975015
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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