A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796166



Internal ID18832254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129234668..129242284hg38UCSC Ensembl
Innerchr9:131996947..132004563hg19UCSC Ensembl
Innerchr9:131036768..131044384hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387617
hg197617
hg187617
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891728
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796166
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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