A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441790



Internal ID22499660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43577819..43578120hg38UCSC Ensembl
chr6:43545556..43545857hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904535
Supporting Variants
Samples
Known GenesPOLH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441790
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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