A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415627



Internal ID21073180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56841918..56842378hg38UCSC Ensembl
chr8:57754477..57754937hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415627
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