A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564194



Internal ID18862475
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 StatusS
Merged Variantsnsv1063958
Supporting Variants
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)nssv3564194
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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