A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438213



Internal ID21095766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33908133..33914479hg38UCSC Ensembl
chr10:34197061..34203407hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv677n223
Supporting Variantsnssv17979797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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