A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355279



Internal ID21012832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102750190..102769633hg38UCSC Ensembl
chr2:103366649..103386092hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3819444
hg1919444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075121
Samples
Known GenesTMEM182
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355279
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