A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136176



Internal ID20703216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93854801..93855700hg38UCSC Ensembl
chr5:93190507..93191406hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411212
Supporting Variants
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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