A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956950



Internal ID18873520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:1209689..1209751hg38UCSC Ensembl
Outerchr3:1251373..1251435hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136700
Supporting Variants
SamplesKWS1
Known GenesCNTN6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956950
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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