A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785246



Internal ID19178021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24152143..24195025hg38UCSC Ensembl
Innerchr7:24191762..24234644hg19UCSC Ensembl
Innerchr7:24158287..24201169hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3842883
hg1942883
hg1842883
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891088
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785246
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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