A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797545



Internal ID19169429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31209671..31255728hg38UCSC Ensembl
Innerchr9:31209669..31255726hg19UCSC Ensembl
Innerchr9:31199669..31245726hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3846058
hg1946058
hg1846058
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891655
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797545
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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