A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122229



Internal ID19264732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67738745..67747133hg38UCSC Ensembl
Outerchr9:46403100..46411500hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388389
hg198401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969672
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122229
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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