A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895014



Internal ID170854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207602089..207602194hg38UCSC Ensembl
chr1:207775434..207775539hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448213
Supporting Variants
Samples
Known GenesCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895014
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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