A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447552



Internal ID21105105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61420734..61421447hg38UCSC Ensembl
chr10:63180492..63181205hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982775
Samples
Known GenesTMEM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447552
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