A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438264



Internal ID216832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14499458..14499825hg38UCSC Ensembl
chr3:14540966..14541333hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930157
Samples
Known GenesGRIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438264
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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