A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332921



Internal ID20866096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145834477..145939081hg38UCSC Ensembl
chr1:145496011..145600635hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38104605
hg19104625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200813
Samples
Known GenesANKRD35, GNRHR2, ITGA10, LIX1L, LOC100288142, MIR6736, NBPF10, NUDT17, PEX11B, PIAS3, POLR3C, RBM8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332921
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