A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036748



Internal ID20603788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54511528..54512347hg38UCSC Ensembl
chr17:52588889..52589708hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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