A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891315



Internal ID18839025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245164783..245720849hg38UCSC Ensembl
Outerchr1:245164783..245720849hg38UCSC Ensembl
Innerchr1:245328085..245884151hg19UCSC Ensembl
Outerchr1:245328085..245884151hg19UCSC Ensembl
Innerchr1:243394708..243950774hg18UCSC Ensembl
Outerchr1:243394708..243950774hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38556067
hg19556067
hg18556067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796075
Samples
Known GenesKIF26B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891315
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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