A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406596



Internal ID21064149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93960654..93961523hg38UCSC Ensembl
chr5:93296359..93297228hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136406
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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