A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396311



Internal ID21053864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93856713..93861946hg38UCSC Ensembl
chr5:93192419..93197652hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136177
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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