A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147564



Internal ID21422310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136429..35137029hg38UCSC Ensembl
chr6:35104206..35104806hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581345
Supporting Variants
SamplesHG00731
Known GenesTCP11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147564
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