A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890794



Internal ID18838410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17623829..17933912hg38UCSC Ensembl
Outerchr6:17623829..17933912hg38UCSC Ensembl
Innerchr6:17624060..17934143hg19UCSC Ensembl
Outerchr6:17624060..17934143hg19UCSC Ensembl
Innerchr6:17732039..18042122hg18UCSC Ensembl
Outerchr6:17732039..18042122hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38310084
hg19310084
hg18310084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789098
Samples
Known GenesKIF13A, NUP153
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890794
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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