A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720899



Internal ID144565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6136129..6142182hg38UCSC Ensembl
chr19:6136140..6142193hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386054
hg196054
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557301
Supporting Variants
Samples
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720899
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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