A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399769



Internal ID21057322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147926213..147949691hg38UCSC Ensembl
chr5:147305776..147329254hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3823479
hg1923479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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