A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583932



Internal ID21775975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66256172..66298599hg38UCSC Ensembl
chr11:66023643..66066070hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3842428
hg1942428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031209
Supporting Variants
Samples
Known GenesCNIH2, KLC2, RAB1B, TMEM151A, YIF1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583932
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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