A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359197



Internal ID22584866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234740285..234742393hg38UCSC Ensembl
chr1:234876032..234878140hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382109
hg192109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359197
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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