A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454188



Internal ID21111741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130237191..130237650hg38UCSC Ensembl
chr10:132035455..132035914hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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