A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640426



Internal ID21588731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185240325..185240325hg38UCSC Ensembl
chr4:186161479..186161479hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131118
SamplesHG00731
Known GenesSNX25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640426
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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