A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153340



Internal ID21448968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72595309..72595309hg38UCSC Ensembl
chr5:71891136..71891136hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635866
Supporting Variants
SamplesHG00864
Known GenesLOC102477328
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153340
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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