A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609252



Internal ID20982323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96860196..96862039hg38UCSC Ensembl
chr6:97308072..97309915hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609252
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