A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153323



Internal ID20720363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128760417..128763718hg38UCSC Ensembl
chr7:128400471..128403772hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433224
Supporting Variants
Samples
Known GenesCALU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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