A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223749



Internal ID20790789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36970001..36977500hg38UCSC Ensembl
chr7:37009606..37017105hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606268
Supporting Variants
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223749
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