A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353862



Internal ID22579531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11041398..11041596hg38UCSC Ensembl
chr1:11101455..11101653hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869554
Supporting Variants
Samples
Known GenesMASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353862
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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