A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456029



Internal ID234099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144326154..144333710hg38UCSC Ensembl
chr6:144647290..144654846hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387557
hg197557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970930
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456029
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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