A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964585



Internal ID19224133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:98068982..98069302hg38UCSC Ensembl
Outerchr13:98721236..98721556hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122855
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964585
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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