A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585694



Internal ID21777737
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 StatusS
Merged Variantsnsv6035745
Supporting Variants
Samples
Known GenesPAMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585694
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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