A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122771



Internal ID21480608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149368760..149368760hg38UCSC Ensembl
chr4:150289912..150289912hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622447
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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