A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037949



Internal ID21947292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58536613..58540035hg38UCSC Ensembl
chr11:58304086..58307508hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg383423
hg193423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585689
Samples
Known GenesLPXN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037949
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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