A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155508



Internal ID20722548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4865693..4969450hg38UCSC Ensembl
chr7:4905324..5009081hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38103758
hg19103758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607201
Supporting Variants
Samples
Known GenesMMD2, RADIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155508
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