A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329088



Internal ID20862239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216983891..217034120hg38UCSC Ensembl
chr1:217157233..217207462hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3850230
hg1950230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200578
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329088
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