A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055178



Internal ID21964411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173613104..173613104hg38UCSC Ensembl
chr1:173582243..173582243hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537141
Samples
Known GenesANKRD45
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055178
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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