A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129063



Internal ID21467350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156189653..156189653hg38UCSC Ensembl
chr3:155907442..155907442hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608234
Supporting Variants
SamplesHG03065
Known GenesKCNAB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129063
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