A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780218



Internal ID19162444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20436571..20480470hg38UCSC Ensembl
Innerchr7:20476194..20520093hg19UCSC Ensembl
Innerchr7:20442719..20486618hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3843900
hg1943900
hg1843900
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891085
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780218
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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