A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432144



Internal ID22490014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6963363..6965719hg38UCSC Ensembl
chr6:6963596..6965952hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382357
hg192357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432144
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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