A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012603



Internal ID21921946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26572111..26624750hg38UCSC Ensembl
chr10:26861040..26913679hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3852640
hg1952640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4n212
Supporting Variantsnssv17590514
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012603
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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