A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671699



Internal ID9937804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72203127..72203920hg38UCSC Ensembl
Outerchr10:72202970..72204073hg38UCSC Ensembl
Innerchr10:73962885..73963678hg19UCSC Ensembl
Outerchr10:73962728..73963831hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6496437
SamplesHG00319
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671699
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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