A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966236



Internal ID22741172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182068991..182068991hg38UCSC Ensembl
chr1:182038126..182038126hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966236
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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