A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624354



Internal ID6664521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99947809..99949554hg38UCSC Ensembl
Innerchr10:99947809..99949554hg38UCSC Ensembl
Outerchr10:99947731..99949649hg38UCSC Ensembl
chr10:101707566..101709311hg19UCSC Ensembl
Innerchr10:101707566..101709311hg19UCSC Ensembl
Outerchr10:101707488..101709406hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381746
hg191746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912290, essv13912291
SamplesHG02882, NA19060
Known GenesDNMBP, DNMBP-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624354
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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