A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506031



Internal ID20879306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16404067..16408974hg38UCSC Ensembl
chr17:16307381..16312288hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384908
hg194908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506031
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