A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413550



Internal ID21071103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148571334..148571960hg38UCSC Ensembl
chr5:147950897..147951523hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125948
Samples
Known GenesHTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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