A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779733



Internal ID19160965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:136834048..136937724hg38UCSC Ensembl
Innerchr2:137591618..137695294hg19UCSC Ensembl
Innerchr2:137308088..137411764hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38103677
hg19103677
hg18103677
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893437
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=40
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779733
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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