A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015408



Internal ID21924751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93855782..93855916hg38UCSC Ensembl
chr5:93191488..93191622hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539811
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015408
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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