A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123139



Internal ID21412361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168155444..168155531hg38UCSC Ensembl
chr4:169076595..169076682hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584216
Supporting Variants
SamplesHG00513
Known GenesANXA10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123139
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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