A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614098



Internal ID20987169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35246101..35248400hg38UCSC Ensembl
chr7:35285713..35288012hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153674
Samples
Known GenesTBX20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614098
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