A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488413



Internal ID265725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137008523..137010082hg38UCSC Ensembl
chr7:136693270..136694829hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381560
hg191560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002788
Samples
Known GenesCHRM2, LOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488413
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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