A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404660



Internal ID21062213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59659867..59697478hg38UCSC Ensembl
chr5:58955693..58993304hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3837612
hg1937612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216466
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404660
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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