A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414706



Internal ID21072259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149560500..149562459hg38UCSC Ensembl
chr5:148940063..148942022hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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