A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622740



Internal ID6662909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28167434..28171324hg38UCSC Ensembl
Innerchr10:28167434..28171324hg38UCSC Ensembl
Outerchr10:28167208..28171523hg38UCSC Ensembl
chr10:28456363..28460253hg19UCSC Ensembl
Innerchr10:28456363..28460253hg19UCSC Ensembl
Outerchr10:28456137..28460452hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383891
hg193891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737820
SamplesHG00556
Known GenesMPP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622740
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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