A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160194



Internal ID20727234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:70206148..70206557hg38UCSC Ensembl
chr7:69671134..69671543hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613601
Supporting Variants
Samples
Known GenesAUTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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