A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960674



Internal ID19204897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:26936074..27010474hg38UCSC Ensembl
Outerchr17:25263100..25337500hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3874401
hg1974401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128761
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960674
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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