A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463828



Internal ID241717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2707206..2708095hg38UCSC Ensembl
chr7:2746840..2747729hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992334
Samples
Known GenesAMZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463828
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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