A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966659



Internal ID22741594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119704984..119704984hg38UCSC Ensembl
chr1:120247607..120247607hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966659
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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