A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971466



Internal ID18894560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113842102..113842159hg38UCSC Ensembl
Outerchr13:114545075..114545132hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122874
Supporting Variants
SamplesKWS2
Known GenesGAS6, GAS6-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971466
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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