A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137494



Internal ID18921167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:104816599..104816651hg38UCSC Ensembl
Outerchr9:107578880..107578932hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976939
SamplesKWS2
Known GenesABCA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137494
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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