A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322457



Internal ID20855570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150980726..150991426hg38UCSC Ensembl
chr1:150953202..150963902hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3810701
hg1910701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200406
Samples
Known GenesANXA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322457
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