A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152173



Internal ID19200476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64401423..64406817hg38UCSC Ensembl
Outerchr9:43096299..43101700hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385395
hg195402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996782
SamplesKWB1
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152173
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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