A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221021



Internal ID20788061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100036439..100045270hg38UCSC Ensembl
chr7:99634062..99642893hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388832
hg198832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610875
Supporting Variants
Samples
Known GenesZKSCAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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