A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462781



Internal ID240703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9727086..9727478hg38UCSC Ensembl
chr6:9727319..9727711hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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