A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135120



Internal ID21467315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144724652..144724652hg38UCSC Ensembl
chr4:145645804..145645804hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612826
Supporting Variants
SamplesHG03065
Known GenesHHIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135120
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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