A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968857



Internal ID19237194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:28617216..28617280hg38UCSC Ensembl
Outerchr13:29191353..29191417hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113552
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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