A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155293



Internal ID20722333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139846101..139983900hg38UCSC Ensembl
chr7:139545900..139683699hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38137800
hg19137800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419061
Supporting Variants
Samples
Known GenesTBXAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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