A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697248



Internal ID21219096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136430..35137030hg38UCSC Ensembl
chr6:35104207..35104807hg19UCSC 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 Variantsnsv2814910
Supporting Variants
Samples
Known GenesTCP11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697248
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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