A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796137



Internal ID19180960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170463121..170493087hg38UCSC Ensembl
Innerchr6:170772209..170802175hg19UCSC Ensembl
Innerchr6:170614134..170644100hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3829967
hg1929967
hg1829967
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891001
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796137
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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