A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441287



Internal ID22499157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24461512..24461620hg38UCSC Ensembl
chr6:24461740..24461848hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887664
Supporting Variants
Samples
Known GenesGPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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