A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989642



Internal ID19243536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:90402277..90425330hg38UCSC Ensembl
Outerchr13:91054531..91077584hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3823054
hg1923054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130910
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989642
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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