A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000769



Internal ID21910112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70517268..70524262hg38UCSC Ensembl
chr10:72277024..72284018hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386995
hg196995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579241
Samples
Known GenesPALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000769
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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