A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438445



Internal ID21095998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60044536..60047977hg38UCSC Ensembl
chr10:61804294..61807735hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg383442
hg193442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982676
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438445
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