A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966679



Internal ID19230971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:43202552..43203352hg38UCSC Ensembl
Outerchr10:43698000..43698800hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112578
Supporting Variants
SamplesKWS2
Known GenesRASGEF1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966679
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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