A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624914



Internal ID7011764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129024800..129026722hg38UCSC Ensembl
Innerchr10:129024823..129026700hg38UCSC Ensembl
Outerchr10:129024778..129026745hg38UCSC Ensembl
chr10:130823064..130824986hg19UCSC Ensembl
Innerchr10:130823087..130824964hg19UCSC Ensembl
Outerchr10:130823042..130825009hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381923
hg191923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13972062
SamplesHG02146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624914
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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