A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446934



Internal ID22504804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42495326..42501135hg38UCSC Ensembl
chr6:42463064..42468873hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385810
hg195810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446934
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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