A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622850



Internal ID6663019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33309330..33321442hg38UCSC Ensembl
Innerchr10:33309346..33321427hg38UCSC Ensembl
Outerchr10:33309315..33321458hg38UCSC Ensembl
chr10:33598258..33610370hg19UCSC Ensembl
Innerchr10:33598274..33610355hg19UCSC Ensembl
Outerchr10:33598243..33610386hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3812113
hg1912113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13751312
SamplesHG00174
Known GenesNRP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622850
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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