A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053653



Internal ID21962886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27487524..27487524hg38UCSC Ensembl
chr1:27814035..27814035hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526549
Samples
Known GenesWASF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053653
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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