A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969660



Internal ID19244137
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 StatusS
Merged Variantsnsv1122216
Supporting Variants
SamplesKWS2
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969660
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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