A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008918



Internal ID21918261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33211287..33211375hg38UCSC Ensembl
chr10:33500215..33500303hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597448
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008918
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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