A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9n100



Internal ID22786096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1696467..1756489hg38UCSC Ensembl
chr1:1627906..1687928hg19UCSC Ensembl
chr1:1617766..1677788hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3860023
hg1960023
hg1860023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007850, nsv998152, nsv1003869
Samples
Known GenesCDK11A, CDK11B, MMP23A, NADK, SLC35E2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv9n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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