A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042677



Internal ID21951989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71100911..71100911hg38UCSC Ensembl
chr1:71566594..71566594hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520130
Samples
Known GenesZRANB2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042677
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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