A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961726



Internal ID19212271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:85071385..85077385hg38UCSC Ensembl
Outerchr9:87686300..87692300hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129053
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961726
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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