A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498079



Internal ID20871287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94447100..94466527hg38UCSC Ensembl
chr15:94990329..95009756hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3819428
hg1919428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027060
Samples
Known GenesMCTP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498079
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