A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799877



Internal ID19169870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58861935..58880160hg38UCSC Ensembl
Innerchr16:58895839..58914064hg19UCSC Ensembl
Innerchr16:57453340..57471565hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3818226
hg1918226
hg1818226
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892866
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799877
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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