A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329086



Internal ID20862237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8475172..8475476hg38UCSC Ensembl
chr1:8535232..8535536hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064770
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329086
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