A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475995



Internal ID253619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95015308..95019829hg38UCSC Ensembl
chr7:94644620..94649141hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384522
hg194522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999688
Samples
Known GenesPPP1R9A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475995
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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