A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435611



Internal ID21093164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18732263..18736396hg38UCSC Ensembl
chr10:19021192..19025325hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg384134
hg194134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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