A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769865



Internal ID19314397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99107745..99108146hg38UCSC Ensembl
chr13:99759999..99760400hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071120
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769865
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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