A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139515



Internal ID18904586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1340005..1343705hg38UCSC Ensembl
Outerchr10:1382200..1385900hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383701
hg193701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977103
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139515
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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