A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891247



Internal ID18838957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158646748..159004277hg38UCSC Ensembl
Outerchr7:158646748..159004277hg38UCSC Ensembl
Innerchr7:158439440..158796968hg19UCSC Ensembl
Outerchr7:158439440..158796968hg19UCSC Ensembl
Innerchr7:158132201..158489729hg18UCSC Ensembl
Outerchr7:158132201..158489729hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38357530
hg19357529
hg18357529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792061
Samples
Known GenesESYT2, NCAPG2, WDR60
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891247
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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