A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087181



Internal ID21996414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71582630..71582630hg38UCSC Ensembl
chr11:71293676..71293676hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594257
Samples
Known GenesKRTAP5-11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087181
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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