A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891103



Internal ID19185499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45719663..45725635hg38UCSC Ensembl
Outerchr7:45719663..45725635hg38UCSC Ensembl
Innerchr7:45759262..45765234hg19UCSC Ensembl
Outerchr7:45759262..45765234hg19UCSC Ensembl
Innerchr7:45725787..45731759hg18UCSC Ensembl
Outerchr7:45725787..45731759hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg385973
hg195973
hg185973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779198
Samples
Known GenesADCY1, SEPT7P2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891103
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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