A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036209



Internal ID20603249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52229796..52230239hg38UCSC Ensembl
chr17:50307156..50307599hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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