A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890637



Internal ID18838035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8955377..8984503hg38UCSC Ensembl
Outerchr1:8955377..8984503hg38UCSC Ensembl
Innerchr1:9015436..9044562hg19UCSC Ensembl
Outerchr1:9015436..9044562hg19UCSC Ensembl
Innerchr1:8938023..8967149hg18UCSC Ensembl
Outerchr1:8938023..8967149hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3829127
hg1929127
hg1829127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789263
Samples
Known GenesCA6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890637
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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