A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891084



Internal ID19185480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19357818..19371666hg38UCSC Ensembl
Outerchr7:19357818..19371666hg38UCSC Ensembl
Innerchr7:19397441..19411289hg19UCSC Ensembl
Outerchr7:19397441..19411289hg19UCSC Ensembl
Innerchr7:19363966..19377814hg18UCSC Ensembl
Outerchr7:19363966..19377814hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813849
hg1913849
hg1813849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800230
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891084
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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