A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556912



Internal ID330031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65053126..65201080hg38UCSC Ensembl
chr1:65518809..65666763hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38147955
hg19147955
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16904540
Samples
Known GenesAK4, MIR101-1, MIR3671
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556912
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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