A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449584



Internal ID21107137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20166701..20168000hg38UCSC Ensembl
chr10:20455630..20456929hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979071
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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