A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778691



Internal ID19169359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63191227..63228092hg38UCSC Ensembl
Innerchr13:63765360..63802225hg19UCSC Ensembl
Innerchr13:62663361..62700226hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3836866
hg1936866
hg1836866
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892372
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778691
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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