A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137667



Internal ID19287040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128689021..128690321hg38UCSC Ensembl
Outerchr9:131451300..131452600hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995027, nssv3969316
SamplesKWS2, KWS1
Known GenesSET
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137667
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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