A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437440



Internal ID21094993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72363591..72364858hg38UCSC Ensembl
chr10:74123349..74124616hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983805
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437440
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