A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448038



Internal ID21105591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70511803..70515446hg38UCSC Ensembl
chr10:72271559..72275202hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383644
hg193644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983532
Samples
Known GenesPALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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