A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414125



Internal ID22471995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13335441..13336919hg38UCSC Ensembl
chr6:13335673..13337151hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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