A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488436



Internal ID265748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149079860..149113802hg38UCSC Ensembl
chr7:148776952..148810894hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3833943
hg1933943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004777
Samples
Known GenesZNF425, ZNF786
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488436
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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