A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159888



Internal ID20726928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91302272..91303102hg38UCSC Ensembl
chr7:90931587..90932417hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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