A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978313



Internal ID19235889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63125128..63144828hg38UCSC Ensembl
Outerchr9:67030100..67049800hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3819701
hg1919701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139977
Supporting Variants
SamplesKWS2
Known GenesLOC286297
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978313
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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