A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436406



Internal ID21093959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6612797..6614184hg38UCSC Ensembl
chr10:6654759..6656146hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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