A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787748



Internal ID19173654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12010374..12110840hg38UCSC Ensembl
Innerchr9:12010374..12110840hg19UCSC Ensembl
Innerchr9:12000374..12100840hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38100467
hg19100467
hg18100467
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891572
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787748
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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