A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322630



Internal ID20855743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201928800..201935753hg38UCSC Ensembl
chr1:201897928..201904881hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386954
hg196954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056650
Samples
Known GenesLMOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer