A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782375



Internal ID19174219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24704690..24729781hg38UCSC Ensembl
Innerchr7:24744309..24769400hg19UCSC Ensembl
Innerchr7:24710834..24735925hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3825092
hg1925092
hg1825092
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891089
Supporting Variants
Samples
Known GenesDFNA5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782375
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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