A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146078



Internal ID345283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2748029..2748651hg38UCSC Ensembl
chr16:2798030..2798652hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706815
Samples
Known GenesSRRM2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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