A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425551



Internal ID21083104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141080410..141082156hg38UCSC Ensembl
chr7:140780210..140781956hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381747
hg191747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150736
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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