A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395653



Internal ID21053206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60412501..60434200hg38UCSC Ensembl
chr5:59708328..59730027hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3821700
hg1921700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5769n223
Supporting Variantsnssv18216231
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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