A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456253



Internal ID234322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94651076..94850520hg38UCSC Ensembl
chr6:95360794..95560238hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38199445
hg19199445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv426n206
Supporting Variantsnssv16988471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456253
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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