A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565623



Internal ID18863904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62198457..62239748hg38UCSC Ensembl
Innerchr18:59865690..59906981hg19UCSC Ensembl
Innerchr18:58016670..58057961hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3841292
hg1941292
hg1841292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055978
Supporting Variants
Samples
Known GenesKIAA1468
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565623
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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