A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443661



Internal ID21101214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17639548..17641050hg38UCSC Ensembl
chr10:17681547..17683049hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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