A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782204



Internal ID19181534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95565624..95588381hg38UCSC Ensembl
Innerchr15:96108853..96131610hg19UCSC Ensembl
Innerchr15:93909857..93932614hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3822758
hg1922758
hg1822758
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892731
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782204
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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