A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990755



Internal ID19232655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26369342..26369408hg38UCSC Ensembl
Outerchr13:26943479..26943545hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138203
Supporting Variants
SamplesKWS2
Known GenesCDK8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990755
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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