A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786351



Internal ID19162886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5661170..5711848hg38UCSC Ensembl
Innerchr6:5661403..5712081hg19UCSC Ensembl
Innerchr6:5606402..5657080hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3850679
hg1950679
hg1850679
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890786
Supporting Variants
Samples
Known GenesFARS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786351
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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