A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030570



Internal ID21939913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72549182..72550376hg38UCSC Ensembl
chr11:72260226..72261420hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030570
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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