A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037009



Internal ID20604049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56496223..56496620hg38UCSC Ensembl
chr17:54573584..54573981hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00113


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer