A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5993644



Internal ID8971047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26927674..27310562hg38UCSC Ensembl
Outerchr10:26927640..27310597hg38UCSC Ensembl
Innerchr10:27216603..27599491hg19UCSC Ensembl
Outerchr10:27216569..27599526hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38382958
hg19382958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664616
Supporting Variants
SamplesHG00121
Known GenesACBD5, ANKRD26, LINC00202-1, LRRC37A6P, MASTL, YME1L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5993644
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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