A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892930



Internal ID19183750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85055589..85061392hg38UCSC Ensembl
Outerchr16:85055589..85061392hg38UCSC Ensembl
Innerchr16:85089195..85094998hg19UCSC Ensembl
Outerchr16:85089195..85094998hg19UCSC Ensembl
Innerchr16:83646696..83652499hg18UCSC Ensembl
Outerchr16:83646696..83652499hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385804
hg195804
hg185804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785792
Samples
Known GenesKIAA0513
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892930
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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