A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352917



Internal ID22578586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224473802..224474594hg38UCSC Ensembl
chr1:224661504..224662296hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352917
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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