A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968323



Internal ID46203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66033859..66033980hg38UCSC Ensembl
chr5:65329687..65329808hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467048
Supporting Variants
Samples
Known GenesERBB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968323
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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