A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138652



Internal ID21462453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112342313..112342363hg38UCSC Ensembl
chr3:112061160..112061210hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566994
Supporting Variants
SamplesHG02818
Known GenesCD200
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138652
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