A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119302



Internal ID19259715
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 StatusM
Merged Variants
Supporting Variantsnssv3959739
SamplesKWS1
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119302
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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