A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523055



Internal ID299304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2755754..2755836hg38UCSC Ensembl
chr16:2805755..2805837hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706818
Samples
Known GenesSRRM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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