A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447647



Internal ID21105200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101370471..101371858hg38UCSC Ensembl
chr10:103130228..103131615hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977193
Samples
Known GenesBTRC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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