A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229369



Internal ID20796409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112226108..112261493hg38UCSC Ensembl
chr7:111866163..111901548hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3835386
hg1935386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612697
Supporting Variants
Samples
Known GenesZNF277
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229369
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