A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447357



Internal ID21104910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12254501..12267300hg38UCSC Ensembl
chr10:12296500..12309299hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv613n223
Supporting Variantsnssv17978221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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