A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447094



Internal ID22504964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21163885..21164557hg38UCSC Ensembl
chr6:21164116..21164788hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893423
Supporting Variants
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447094
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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