A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988724



Internal ID20555764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19709745..19711327hg38UCSC Ensembl
chr11:19731291..19732873hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381583
hg191583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437818
Supporting Variants
Samples
Known GenesLOC100126784, NAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988724
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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