A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156298



Internal ID15878151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14281798..14300104hg38UCSC Ensembl
Innerchr8:14139307..14157613hg19UCSC Ensembl
Innerchr8:14183678..14201984hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3818307
hg1918307
hg1818307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610463
Supporting Variants
SamplesHGDP01102
Known GenesSGCZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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