A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796079



Internal ID18815110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22600363..23220738hg38UCSC Ensembl
Innerchr15:22652330..23272733hg19UCSC Ensembl
Innerchr15:20203694..20824174hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38620376
hg19620404
hg18620481
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892626
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8I, LOC283683, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=104
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796079
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer