A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782270



Internal ID18828760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387541..31489965hg38UCSC Ensembl
Innerchr6:31355318..31457742hg19UCSC Ensembl
Innerchr6:31463297..31565721hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38102425
hg19102425
hg18102425
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=175
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782270
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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