A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382756



Internal ID21040309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36286306..36291146hg38UCSC Ensembl
chr5:36286408..36291248hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg384841
hg194841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131939
Samples
Known GenesRANBP3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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