A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559044



Internal ID332090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107230760..107230778hg38UCSC Ensembl
chr1:107773382..107773400hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819
hg1919
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16907956
Samples
Known GenesNTNG1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559044
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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