A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976676



Internal ID19229564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:80655644..80659444hg38UCSC Ensembl
Outerchr10:82415400..82419200hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg383801
hg193801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124622
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976676
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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