A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782238



Internal ID19172626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:209136074..209160214hg38UCSC Ensembl
Innerchr2:210000798..210024938hg19UCSC Ensembl
Innerchr2:209709043..209733183hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3824141
hg1924141
hg1824141
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 HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782238
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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