A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320596



Internal ID20853695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91491401..91573200hg38UCSC Ensembl
chr1:91956958..92038757hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3881800
hg1981800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203159
Samples
Known GenesCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320596
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