A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798866



Internal ID18829851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10481967..10495488hg38UCSC Ensembl
Innerchr16:10575824..10589345hg19UCSC Ensembl
Innerchr16:10483325..10496846hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3813522
hg1913522
hg1813522
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892790
Supporting Variants
Samples
Known GenesATF7IP2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798866
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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