A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779564



Internal ID19173857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100160601..100367374hg38UCSC Ensembl
Innerchr13:100812855..101019628hg19UCSC Ensembl
Innerchr13:99610856..99817629hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38206774
hg19206774
hg18206774
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=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779564
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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