A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768863



Internal ID19313255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:172596891..172596980hg38UCSC Ensembl
Outerchr5:172023894..172023983hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078245
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768863
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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