A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778768



Internal ID18819337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31905688..31910718hg38UCSC Ensembl
Innerchr6:31873465..31878495hg19UCSC Ensembl
Innerchr6:31981444..31986474hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385031
hg195031
hg185031
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890823
Supporting Variants
Samples
Known GenesC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778768
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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