A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231866



Internal ID20798906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140363601..140432200hg38UCSC Ensembl
chr7:140063401..140132000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3868600
hg1968600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431247
Supporting Variants
Samples
Known GenesRAB19, SLC37A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231866
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