A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368877



Internal ID22594546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127071222..127071222hg38UCSC Ensembl
chr11:126941117..126941117hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368877
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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