A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976614



Internal ID19246488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:12490546..12493046hg38UCSC Ensembl
Outerchr1:12550600..12553100hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124560
Supporting Variants
SamplesKWS2
Known GenesVPS13D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976614
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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