A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786077



Internal ID19166024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95885020..96058284hg38UCSC Ensembl
Innerchr13:96537274..96710538hg19UCSC Ensembl
Innerchr13:95335275..95508539hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38173265
hg19173265
hg18173265
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892431
Supporting Variants
Samples
Known GenesUGGT2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786077
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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