A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787062



Internal ID19174590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:874129..879935hg38UCSC Ensembl
Innerchr9:874129..879935hg19UCSC Ensembl
Innerchr9:864129..869935hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg385807
hg195807
hg185807
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891515
Supporting Variants
Samples
Known GenesDMRT1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787062
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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