A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891030



Internal ID18838740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5841662..5888325hg38UCSC Ensembl
Outerchr7:5841662..5888325hg38UCSC Ensembl
Innerchr7:5881293..5927956hg19UCSC Ensembl
Outerchr7:5881293..5927956hg19UCSC Ensembl
Innerchr7:5847819..5894482hg18UCSC Ensembl
Outerchr7:5847819..5894482hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3846664
hg1946664
hg1846664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779775
Samples
Known GenesOCM, ZNF815P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891030
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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