A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122216



Internal ID19260419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40223882..40225782hg38UCSC Ensembl
Outerchr9:42368900..42370800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969660
SamplesKWS2
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122216
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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