A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782771



Internal ID19182739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64081079..64569806hg38UCSC Ensembl
Innerchr13:64655212..65143938hg19UCSC Ensembl
Innerchr13:63553213..64041939hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38488728
hg19488727
hg18488727
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892366
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=64
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782771
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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