A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044724



Internal ID21954006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2028326..2028326hg38UCSC Ensembl
chr1:1959765..1959765hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526384
Samples
Known GenesGABRD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044724
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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