A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087637



Internal ID21996870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63893357..63893357hg38UCSC Ensembl
chr11:63660829..63660829hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594737
Samples
Known GenesMARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087637
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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