A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055632



Internal ID18798163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59674657..59934231hg38UCSC Ensembl
Innerchr18:57341889..57601463hg19UCSC Ensembl
Innerchr18:55492869..55752443hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38259575
hg19259575
hg18259575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565496
Samples
Known GenesCCBE1, PMAIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055632
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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