A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977103



Internal ID18900263
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 StatusS
Merged Variantsnsv1139515
Supporting Variants
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977103
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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