A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789590



Internal ID19160659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32516591hg38UCSC Ensembl
Innerchr6:32455482..32484368hg19UCSC Ensembl
Innerchr6:32563460..32592346hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3828887
hg1928887
hg1828887
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890830
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789590
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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