A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152611



Internal ID20719651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126693247..126726606hg38UCSC Ensembl
chr7:126333301..126366660hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3833360
hg1933360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418184
Supporting Variants
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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