A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989350



Internal ID18883308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1409923..1410043hg38UCSC Ensembl
Outerchr10:1452118..1452238hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135763
Supporting Variants
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989350
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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