A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966960



Internal ID18883229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26710091..26713240hg38UCSC Ensembl
Outerchr10:26999020..27002169hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130645
Supporting Variants
SamplesKWS2
Known GenesPDSS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966960
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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