A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414785



Internal ID21072338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58644539..58659925hg38UCSC Ensembl
chr5:57940366..57955752hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3815387
hg1915387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133683
Samples
Known GenesRAB3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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