A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783796



Internal ID19167447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61632502..61655297hg38UCSC Ensembl
Innerchr5:60928329..60951124hg19UCSC Ensembl
Innerchr5:60964086..60986881hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3822796
hg1922796
hg1822796
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894197
Supporting Variants
Samples
Known GenesC5orf64
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783796
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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