A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059592



Internal ID19148811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36959202..37006782hg38UCSC Ensembl
Innerchr18:34539165..34586745hg19UCSC Ensembl
Innerchr18:32793163..32840743hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3847581
hg1947581
hg1847581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564205, nssv3564206
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059592
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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