A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994125



Internal ID19210740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:41987509..41987561hg38UCSC Ensembl
Outerchr6:41955247..41955299hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142638
Supporting Variants
SamplesKWS1
Known GenesCCND3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994125
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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