A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786619



Internal ID19166051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30816586..30887331hg38UCSC Ensembl
Innerchr15:31108789..31179534hg19UCSC Ensembl
Innerchr15:28896081..28966826hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3870746
hg1970746
hg1870746
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892647
Supporting Variants
Samples
Known GenesHERC2P10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786619
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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