A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352450



Internal ID22578119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218850731..218855836hg38UCSC Ensembl
chr1:219024073..219029178hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385106
hg195106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352450
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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