A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485389



Internal ID262779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146532504..146798644hg38UCSC Ensembl
chr7:146229596..146495736hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38266141
hg19266141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006457
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485389
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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