A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417862



Internal ID22475732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13528099..13528192hg38UCSC Ensembl
chr6:13528331..13528424hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907308
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417862
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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