A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786549



Internal ID19169786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35934461..36050028hg38UCSC Ensembl
Innerchr16:35168832..35284399hg19UCSC Ensembl
Innerchr16:35026333..35141900hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38115568
hg19115568
hg18115568
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892854
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786549
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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