A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799191



Internal ID19182966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160608696..160634795hg38UCSC Ensembl
Innerchr6:161029728..161055827hg19UCSC Ensembl
Innerchr6:160949718..160975817hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3826100
hg1926100
hg1826100
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890975
Supporting Variants
Samples
Known GenesLPA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799191
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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