A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782755



Internal ID19173078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24231248..24292585hg38UCSC Ensembl
Innerchr9:24231246..24292583hg19UCSC Ensembl
Innerchr9:24221246..24282583hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3861338
hg1961338
hg1861338
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891640
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782755
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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