A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461649



Internal ID22519534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183614636..183619597hg38UCSC Ensembl
chr1:183583771..183588732hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg384962
hg194962
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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