A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147092



Internal ID346285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229416418..229416778hg38UCSC Ensembl
chr1:229552165..229552525hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16898329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147092
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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