A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799667



Internal ID19171570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61632502..61661308hg38UCSC Ensembl
Innerchr5:60928329..60957135hg19UCSC Ensembl
Innerchr5:60964086..60992892hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3828807
hg1928807
hg1828807
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=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799667
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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