A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038058



Internal ID20605098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7201197..7203279hg38UCSC Ensembl
chr17:7104516..7106598hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382083
hg192083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509282
Supporting Variants
Samples
Known GenesDLG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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