A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961003



Internal ID18864353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:73119219..73143342hg38UCSC Ensembl
Outerchr10:74878977..74903100hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3824124
hg1924124
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120224
Supporting Variants
SamplesKWS1
Known GenesECD, NUDT13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961003
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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