A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091010



Internal ID22000243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60281288..60281288hg38UCSC Ensembl
chr12:60675069..60675069hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091010
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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