A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015888



Internal ID19105106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4787550..4883429hg38UCSC Ensembl
Innerchr6:4787784..4883663hg19UCSC Ensembl
Innerchr6:4732783..4828662hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3895880
hg1995880
hg1895880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747905
Samples
Known GenesCDYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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