A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041811



Internal ID21951141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8235043..8235127hg38UCSC Ensembl
chrUn_gl000220:133459..133543hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041811
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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