A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454067



Internal ID21111620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124483987..124484297hg38UCSC Ensembl
chr10:126172556..126172866hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978009
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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