A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431458



Internal ID21089011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126668799..126669889hg38UCSC Ensembl
chr7:126308853..126309943hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233037
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431458
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