A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747905



Internal ID19046186
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 StatusS
Merged Variantsnsv1015888
Supporting Variants
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)nssv3747905
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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