A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891190



Internal ID19185586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111839068..111910331hg38UCSC Ensembl
Outerchr7:111839068..111910331hg38UCSC Ensembl
Innerchr7:111479124..111550387hg19UCSC Ensembl
Outerchr7:111479124..111550387hg19UCSC Ensembl
Innerchr7:111266360..111337623hg18UCSC Ensembl
Outerchr7:111266360..111337623hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3871264
hg1971264
hg1871264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786431
Samples
Known GenesDOCK4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891190
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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