A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953840



Internal ID36566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92051625..92545686hg38UCSC Ensembl
chr4:92972776..93466837hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38494062
hg19494062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456419
Supporting Variants
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953840
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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