A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958860



Internal ID19222760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128794507..128795492hg38UCSC Ensembl
Outerchr9:131556786..131557771hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118371
Supporting Variants
SamplesKWS1
Known GenesTBC1D13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958860
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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