A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156149



Internal ID20723189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32888710..32889254hg38UCSC Ensembl
chr7:32928322..32928866hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617411
Supporting Variants
Samples
Known GenesKBTBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156149
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