A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087671



Internal ID21996904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44164607..44164607hg38UCSC Ensembl
chr13:44738743..44738743hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087671
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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