A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115176



Internal ID18935367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:37918362..37918422hg38UCSC Ensembl
Outerchr9:37918359..37918419hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976226
SamplesKWS2
Known GenesSHB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115176
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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