A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891150



Internal ID19185546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80519352..80526998hg38UCSC Ensembl
Outerchr7:80519352..80526998hg38UCSC Ensembl
Innerchr7:80148668..80156314hg19UCSC Ensembl
Outerchr7:80148668..80156314hg19UCSC Ensembl
Innerchr7:79986604..79994250hg18UCSC Ensembl
Outerchr7:79986604..79994250hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387647
hg197647
hg187647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785007, essv25801555
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891150
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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