A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123335



Internal ID20690375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100463901..100574900hg38UCSC Ensembl
chr5:99799605..99910604hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38111000
hg19111000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407992
Supporting Variants
Samples
Known GenesFAM174A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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