A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145013



Internal ID21481483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70594900..70595019hg38UCSC Ensembl
chr6:71304603..71304722hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566225
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145013
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