A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137664



Internal ID18936768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97983818..97985118hg38UCSC Ensembl
Outerchr9:100746100..100747400hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990166
SamplesKWS2
Known GenesANP32B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137664
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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