A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008212



Internal ID21917555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5423418..5424801hg38UCSC Ensembl
chr10:5465381..5466764hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596122
Samples
Known GenesNET1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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