A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444516



Internal ID21102069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28273701..28283700hg38UCSC Ensembl
chr10:28562630..28572629hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981286
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444516
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