A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797855



Internal ID19173634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:209136074..209160213hg38UCSC Ensembl
Innerchr2:210000798..210024937hg19UCSC Ensembl
Innerchr2:209709043..209733182hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3824140
hg1924140
hg1824140
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893541
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797855
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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