A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573191



Internal ID21765234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5692433..5706702hg38UCSC Ensembl
chr6:5692666..5706935hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3814270
hg1914270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019391
Supporting Variants
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573191
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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