A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779323



Internal ID19162520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14541650..14551811hg38UCSC Ensembl
Innerchr2:14681774..14691935hg19UCSC Ensembl
Innerchr2:14599225..14609386hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3810162
hg1910162
hg1810162
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891559
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779323
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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