A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770573



Internal ID19311950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32427062..32429463hg38UCSC Ensembl
chr13:33001199..33003600hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070164
Supporting Variants
SamplesKWP1
Known GenesN4BP2L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770573
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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