A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423760



Internal ID21081313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30665536..30706589hg38UCSC Ensembl
chr8:30523053..30564106hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3841054
hg1941054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234138
Samples
Known GenesGSR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423760
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