A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785092



Internal ID19171782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95782414..95801846hg38UCSC Ensembl
Innerchr15:96325643..96345075hg19UCSC Ensembl
Innerchr15:94126647..94146079hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3819433
hg1919433
hg1819433
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892732
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785092
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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