A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160372



Internal ID20727412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:827755..831494hg38UCSC Ensembl
chr7:867392..871131hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383740
hg193740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619328
Supporting Variants
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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