A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049524



Internal ID21958757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6937340..6937340hg38UCSC Ensembl
chr1:6997400..6997400hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533829
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049524
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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