A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062418



Internal ID21432932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201690165..201690381hg38UCSC Ensembl
chr1:201659293..201659509hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569709
Supporting Variants
SamplesHG00731
Known GenesIPO9-AS1, NAV1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062418
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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