A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891018



Internal ID19185414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3671119..3714320hg38UCSC Ensembl
Outerchr7:3671119..3714320hg38UCSC Ensembl
Innerchr7:3710751..3753952hg19UCSC Ensembl
Outerchr7:3710751..3753952hg19UCSC Ensembl
Innerchr7:3677277..3720478hg18UCSC Ensembl
Outerchr7:3677277..3720478hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3843202
hg1943202
hg1843202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780386
Samples
Known GenesSDK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891018
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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