A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610663



Internal ID21558968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7510717..7510717hg38UCSC Ensembl
chr4:7512444..7512444hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126661
SamplesNA20509
Known GenesSORCS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610663
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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