A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450958



Internal ID22508831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34479641..34480682hg38UCSC Ensembl
chr1:34945242..34946283hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450958
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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