A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783817



Internal ID19168668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57577944..57602766hg38UCSC Ensembl
Innerchr16:57611856..57636678hg19UCSC Ensembl
Innerchr16:56169357..56194179hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3824823
hg1924823
hg1824823
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892865
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783817
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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