A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891033



Internal ID19185429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6804091..6909016hg38UCSC Ensembl
Outerchr7:6804091..6909016hg38UCSC Ensembl
Innerchr7:6843722..6948647hg19UCSC Ensembl
Outerchr7:6843722..6948647hg19UCSC Ensembl
Innerchr7:6810247..6915172hg18UCSC Ensembl
Outerchr7:6810247..6915172hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38104926
hg19104926
hg18104926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792514
Samples
Known GenesCCZ1B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891033
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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