A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035745



Internal ID21945088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35501466..35505586hg38UCSC Ensembl
chr11:35523014..35527134hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384121
hg194121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585694
Samples
Known GenesPAMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035745
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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