A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461272



Internal ID22519155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41724257..41726306hg38UCSC Ensembl
chr1:42189928..42191977hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382050
hg192050
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830319
Supporting Variants
Samples
Known GenesHIVEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461272
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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