A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892300



Internal ID18836434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19728834..19868739hg38UCSC Ensembl
Outerchr13:19728834..19868739hg38UCSC Ensembl
Innerchr13:20302974..20442879hg19UCSC Ensembl
Outerchr13:20302974..20442879hg19UCSC Ensembl
Innerchr13:19200974..19340879hg18UCSC Ensembl
Outerchr13:19200974..19340879hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38139906
hg19139906
hg18139906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784661
Samples
Known GenesPSPC1, ZMYM5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892300
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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