A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8n100



Internal ID20151624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1569349..1741152hg38UCSC Ensembl
chr1:1504729..1672591hg19UCSC Ensembl
chr1:1494592..1662451hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38171804
hg19167863
hg18167860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002038, nsv1011271
Samples
Known GenesC1orf233, CDK11A, CDK11B, MIB2, MMP23A, MMP23B, SLC35E2, SLC35E2B, SSU72
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv8n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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