A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893179



Internal ID19183999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21236750..21304570hg38UCSC Ensembl
Outerchr19:21236750..21304570hg38UCSC Ensembl
Innerchr19:21419552..21487372hg19UCSC Ensembl
Outerchr19:21419552..21487372hg19UCSC Ensembl
Innerchr19:21211392..21279212hg18UCSC Ensembl
Outerchr19:21211392..21279212hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3867821
hg1967821
hg1867821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779793
Samples
Known GenesZNF708
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893179
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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