A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147451



Internal ID346632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5395255..5396566hg38UCSC Ensembl
chr5:5395368..5396679hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147451
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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