A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154526



Internal ID20721566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42941740..42942695hg38UCSC Ensembl
chr7:42981339..42982294hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610493
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154526
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