A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892626



Internal ID18836760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22600363..22914964hg38UCSC Ensembl
Outerchr15:22358243..23220738hg38UCSC Ensembl
Innerchr15:22958104..23272733hg19UCSC Ensembl
Outerchr15:22652330..23585019hg19UCSC Ensembl
Innerchr15:20509545..20824174hg18UCSC Ensembl
Outerchr15:20203694..21136460hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38862496
hg19932690
hg18932767
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796079, essv25790870, essv25791905
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8EP, GOLGA8I, HERC2P2, HERC2P7, LOC283683, LOC440243, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892626
Frequency
Sample Size3017
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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