A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407580



Internal ID21065133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148596306..148605722hg38UCSC Ensembl
chr5:147975869..147985285hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg389417
hg199417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213272
Samples
Known GenesHTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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