A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130518



Internal ID21454806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187304398..187304398hg38UCSC Ensembl
chr4:188225552..188225552hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633174
Supporting Variants
SamplesHG02011
Known GenesLOC339975
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130518
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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