A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035606



Internal ID20602646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33239347..33247368hg38UCSC Ensembl
chr17:31566365..31574386hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg388022
hg198022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513221
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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