A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034492



Internal ID18777026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98424113..98444288hg38UCSC Ensembl
Innerchr8:99436341..99456516hg19UCSC Ensembl
Innerchr8:99505517..99525692hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3820176
hg1920176
hg1820176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689740
Samples
Known GenesKCNS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034492
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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