A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968626



Internal ID18883492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:70288664..70289864hg38UCSC Ensembl
Outerchr18:67955900..67957100hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121954
Supporting Variants
SamplesKWS2
Known GenesSOCS6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968626
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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