A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395156



Internal ID22453026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127308884..127309033hg38UCSC Ensembl
chr3:127027727..127027876hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889750
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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