A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800575



Internal ID18817954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450638..34496365hg38UCSC Ensembl
Innerchr15:34742839..34788566hg19UCSC Ensembl
Innerchr15:32530131..32575858hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3845728
hg1945728
hg1845728
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892663
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800575
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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