A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143402



Internal ID20710442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42910305..42924714hg38UCSC Ensembl
chr6:42878043..42892452hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3814410
hg1914410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408355
Supporting Variants
Samples
Known GenesPTCRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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