A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797175



Internal ID18830744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30648195..30675803hg38UCSC Ensembl
Innerchr15:30940398..30968006hg19UCSC Ensembl
Innerchr15:28727690..28755298hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3827609
hg1927609
hg1827609
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892646
Supporting Variants
Samples
Known GenesLOC100288637
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797175
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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