A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017509



Internal ID21926852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26584051..26639261hg38UCSC Ensembl
chr10:26872980..26928190hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3855211
hg1955211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4n212
Supporting Variantsnssv17593484
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017509
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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