A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993592



Internal ID18895703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1473941..1474070hg38UCSC Ensembl
Outerchr10:1516136..1516265hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142086
Supporting Variants
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993592
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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