A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961603



Internal ID19213476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:25744180..25750380hg38UCSC Ensembl
Outerchr7:25783800..25790000hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg386201
hg196201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128933
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961603
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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