A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624444



Internal ID7011299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105341005..105558140hg38UCSC Ensembl
Innerchr10:105341155..105557990hg38UCSC Ensembl
Outerchr10:105340855..105558290hg38UCSC Ensembl
chr10:107100763..107317898hg19UCSC Ensembl
Innerchr10:107100913..107317748hg19UCSC Ensembl
Outerchr10:107100613..107318048hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38217136
hg19217136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13919366, essv13919367, essv13919368
SamplesHG02789, HG02725, HG02684
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624444
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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