A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212429



Internal ID20779469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112836261..112851125hg38UCSC Ensembl
chr5:112171958..112186822hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3814865
hg1914865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413479
Supporting Variants
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212429
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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