A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947244



Internal ID32192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39317851..39317938hg38UCSC Ensembl
chr4:39319471..39319558hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459774
Supporting Variants
Samples
Known GenesMIR1273H, RFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947244
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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