A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006195



Internal ID71756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135588200..135590383hg38UCSC Ensembl
chr7:135272948..135275131hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382184
hg192184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477980
Supporting Variants
Samples
Known GenesNUP205
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006195
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.037153


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