A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982002



Internal ID19223950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35605303..35605603hg38UCSC Ensembl
Outerchr9:35605300..35605600hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119196
Supporting Variants
SamplesKWS1
Known GenesTESK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982002
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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