A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035241



Internal ID20602281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37637290..37637765hg38UCSC Ensembl
chr17:35997320..35997795hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509989
Supporting Variants
Samples
Known GenesDDX52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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