A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132541



Internal ID21481695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6037938..6038105hg38UCSC Ensembl
chr4:6039665..6039832hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584469
Supporting Variants
SamplesHG03683
Known GenesJAKMIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132541
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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