A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894955



Internal ID170811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206911039..206911107hg38UCSC Ensembl
chr1:207084384..207084452hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438329
Supporting Variants
Samples
Known GenesFAIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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