A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414743



Internal ID22472613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159241788..159242591hg38UCSC Ensembl
chr6:159662820..159663623hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898811
Supporting Variants
Samples
Known GenesFNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414743
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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