A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16898485



Internal ID173125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238293258..238293258hg38UCSC Ensembl
chr1:238456558..238456558hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16898485
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.021256


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