A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800519



Internal ID19163662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65058204..65148152hg38UCSC Ensembl
Innerchr13:65632336..65722284hg19UCSC Ensembl
Innerchr13:64530337..64620285hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3889949
hg1989949
hg1889949
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892374
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800519
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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