A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421300



Internal ID22479170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133707808..133715117hg38UCSC Ensembl
chr6:134028946..134036255hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387310
hg197310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421300
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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