A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13912290



Internal ID3914106
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624354
Supporting Variants
SamplesHG02882
Known GenesDNMBP, DNMBP-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13912290
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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