A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800295



Internal ID19161194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:93610953..93687573hg38UCSC Ensembl
Innerchr13:94263206..94339826hg19UCSC Ensembl
Innerchr13:93061207..93137827hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3876621
hg1976621
hg1876621
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892428
Supporting Variants
Samples
Known GenesGPC6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800295
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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