A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960959



Internal ID18864034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69189584..69190084hg38UCSC Ensembl
Outerchr9:71804500..71805000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120191
Supporting Variants
SamplesKWS1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960959
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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