A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440677



Internal ID21098230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16335903..16352762hg38UCSC Ensembl
chr10:16377902..16394761hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3816860
hg1916860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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