A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063958



Internal ID19153177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33282753..33351652hg38UCSC Ensembl
Innerchr18:30862717..30931616hg19UCSC Ensembl
Innerchr18:29116715..29185614hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3868900
hg1968900
hg1868900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564194
Samples
Known GenesCCDC178
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063958
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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