A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454828



Internal ID22512705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45164247..45168288hg38UCSC Ensembl
chr1:45629919..45633960hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg384042
hg194042
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830330
Supporting Variants
Samples
Known GenesZSWIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454828
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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