A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785398



Internal ID19173117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100160601..100357200hg38UCSC Ensembl
Innerchr13:100812855..101009454hg19UCSC Ensembl
Innerchr13:99610856..99807455hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38196600
hg19196600
hg18196600
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892434
Supporting Variants
Samples
Known GenesPCCA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785398
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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