A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800219



Internal ID19174910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160810560..160833648hg38UCSC Ensembl
Innerchr6:161231592..161254680hg19UCSC Ensembl
Innerchr6:161151582..161174670hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3823089
hg1923089
hg1823089
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890976
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800219
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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