A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538007



Internal ID313179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98288134..98288134hg38UCSC Ensembl
chr4:99209285..99209285hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954251
Samples
Known GenesRAP1GDS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538007
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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