A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125521



Internal ID20692561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122360264..122360590hg38UCSC Ensembl
chr5:121695959..121696285hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409294
Supporting Variants
Samples
Known GenesSNCAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00155


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