A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152666



Internal ID20719706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127159723..127169635hg38UCSC Ensembl
chr7:126799777..126809689hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg389913
hg199913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418901
Supporting Variants
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00123


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