A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778794



Internal ID18823752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27771601..27814760hg38UCSC Ensembl
Innerchr6:27739380..27782538hg19UCSC Ensembl
Innerchr6:27847359..27890517hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3843160
hg1943159
hg1843159
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890803
Supporting Variants
Samples
Known GenesHIST1H2AI, HIST1H2AJ, HIST1H2BL, HIST1H3H
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778794
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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