A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530981



Internal ID20904342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57688243..57688769hg38UCSC Ensembl
chr17:55765604..55766130hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530981
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