A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454006



Internal ID22511881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203439650..203444509hg38UCSC Ensembl
chr1:203408778..203413637hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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