A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333423



Internal ID20866599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66180601..66184900hg38UCSC Ensembl
chr1:66646284..66650583hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv219n223
Supporting Variantsnssv18062537
Samples
Known GenesPDE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333423
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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