A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956602



Internal ID38378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146407017..146409885hg38UCSC Ensembl
chr4:147328169..147331037hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg382869
hg192869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471596
Supporting Variants
Samples
Known GenesMIR7849, SLC10A7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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