A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355268



Internal ID22580937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66136193..66137249hg38UCSC Ensembl
chr11:65903664..65904720hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381057
hg191057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910350
Supporting Variants
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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