A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640956



Internal ID21589261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186433229..186433229hg38UCSC Ensembl
chr4:187354383..187354383hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg384186
hg194186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129668, nssv17129286, nssv17123754
SamplesHG00512, HG00864
Known GenesF11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640956
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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