A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144510



Internal ID343715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74732719..74732839hg38UCSC Ensembl
chr17:72728858..72728978hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714570
Samples
Known GenesRAB37
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144510
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer