A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228998



Internal ID20796038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29628701..29659200hg38UCSC Ensembl
chr7:29668317..29698816hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3830500
hg1930500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614663
Supporting Variants
Samples
Known GenesLOC646762
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00034


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