A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416742



Internal ID21074295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159129634..159245836hg38UCSC Ensembl
chr7:158922325..159038526hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38116203
hg19116202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7209n223
Supporting Variantsnssv18229441
Samples
Known GenesVIPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416742
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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