A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959443



Internal ID19206560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49246155..49250455hg38UCSC Ensembl
Outerchr10:50454200..50458500hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384301
hg194301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110176
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959443
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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