A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947233



Internal ID32184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39160987..39161038hg38UCSC Ensembl
chr4:39162607..39162658hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140925
Supporting Variants
Samples
Known GenesMIR1273H
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947233
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.259244


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