A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441193



Internal ID21098746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43801186..43830371hg38UCSC Ensembl
chr10:44296634..44325819hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3829186
hg1929186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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