A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983376



Internal ID19214055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:90263348..90295394hg38UCSC Ensembl
Outerchr13:90915602..90947648hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3832047
hg1932047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145688
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983376
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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