A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891141



Internal ID18838851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71585497..71603268hg38UCSC Ensembl
Outerchr7:71585497..71603268hg38UCSC Ensembl
Innerchr7:71050482..71068253hg19UCSC Ensembl
Outerchr7:71050482..71068253hg19UCSC Ensembl
Innerchr7:70688418..70706189hg18UCSC Ensembl
Outerchr7:70688418..70706189hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3817772
hg1917772
hg1817772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779029
Samples
Known GenesWBSCR17
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891141
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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