A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064487



Internal ID19153706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6487466..6520581hg38UCSC Ensembl
Innerchr18:6487465..6520580hg19UCSC Ensembl
Innerchr18:6477465..6510580hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3833116
hg1933116
hg1833116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564086, nssv3564085
Samples
Known GenesC18orf64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064487
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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