A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764943



Internal ID19304711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41693522..41856406hg38UCSC Ensembl
Outerchr10:42383803..42599540hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38162885
hg19215738
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076766
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764943
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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