A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624353



Internal ID7011209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99935832..99938751hg38UCSC Ensembl
Innerchr10:99935871..99938712hg38UCSC Ensembl
Outerchr10:99935793..99938790hg38UCSC Ensembl
chr10:101695589..101698508hg19UCSC Ensembl
Innerchr10:101695628..101698469hg19UCSC Ensembl
Outerchr10:101695550..101698547hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382920
hg192920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912289
SamplesHG02786
Known GenesDNMBP, DNMBP-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624353
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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