A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044137



Internal ID21953428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247129927..247129927hg38UCSC Ensembl
chr1:247293229..247293229hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528818
Samples
Known GenesZNF124
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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