A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987479



Internal ID19207973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40262382..40269082hg38UCSC Ensembl
Outerchr9:42407400..42414100hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386701
hg196701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132689
Supporting Variants
SamplesKWS1
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987479
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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