A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959739



Internal ID19224155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67869154..67886454hg38UCSC Ensembl
Outerchr9:67936600..67953900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3817301
hg1917301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119302
Supporting Variants
SamplesKWS1
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959739
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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