A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786078



Internal ID18825068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71809756..72033254hg38UCSC Ensembl
Innerchr15:72102096..72325595hg19UCSC Ensembl
Innerchr15:69889150..70112649hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38223499
hg19223500
hg18223500
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892712
Supporting Variants
Samples
Known GenesMYO9A, NR2E3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=38
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786078
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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