A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056985



Internal ID18799516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32906308..32960383hg38UCSC Ensembl
Innerchr18:30486272..30540347hg19UCSC Ensembl
Innerchr18:28740270..28794345hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3854076
hg1954076
hg1854076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3333n100
Supporting Variantsnssv3564192
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)nsv1056985
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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