A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439048



Internal ID21096601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6494525..6501860hg38UCSC Ensembl
chr11:6515755..6523090hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387336
hg197336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994073
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439048
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