A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961703



Internal ID19216569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63112928..63120728hg38UCSC Ensembl
Outerchr9:67017900..67025700hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg387801
hg197801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129030
Supporting Variants
SamplesKWS1
Known GenesLOC286297
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961703
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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