A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969060



Internal ID19238596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:325656..328856hg38UCSC Ensembl
Outerchr20:306300..309500hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133498
Supporting Variants
SamplesKWS2
Known GenesSOX12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969060
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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