A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436876



Internal ID21094429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26602401..26682100hg38UCSC Ensembl
chr10:26891330..26971029hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3879700
hg1979700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv663n223
Supporting Variantsnssv17981181
Samples
Known GenesLINC00202-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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