A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143404



Internal ID20710444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42920493..42921486hg38UCSC Ensembl
chr6:42888231..42889224hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405381
Supporting Variants
Samples
Known GenesPTCRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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