A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892423



Internal ID19183243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91772754..91936572hg38UCSC Ensembl
Outerchr13:91772754..91936572hg38UCSC Ensembl
Innerchr13:92425008..92588826hg19UCSC Ensembl
Outerchr13:92425008..92588826hg19UCSC Ensembl
Innerchr13:91223009..91386827hg18UCSC Ensembl
Outerchr13:91223009..91386827hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38163819
hg19163819
hg18163819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784265
Samples
Known GenesGPC5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892423
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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