A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956702



Internal ID38442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126513213..126612869hg38UCSC Ensembl
chr4:127434368..127534024hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3899657
hg1999657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956702
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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