A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101325



Internal ID21428921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58863530..58863530hg38UCSC Ensembl
chr18:56530762..56530762hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660953
Supporting Variants
SamplesHG00731
Known GenesZNF532
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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