A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392307



Internal ID21049860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6659196..6664406hg38UCSC Ensembl
chr5:6659309..6664519hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133915
Samples
Known GenesSRD5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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