A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625963



Internal ID21574268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131785111..131785111hg38UCSC Ensembl
chr5:131120804..131120804hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136706
SamplesHG00731
Known GenesFNIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625963
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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