A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801169



Internal ID18823672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31485841hg38UCSC Ensembl
Innerchr6:31360389..31453618hg19UCSC Ensembl
Innerchr6:31468368..31561597hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3893230
hg1993230
hg1893230
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890819
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=166
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801169
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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