A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469617



Internal ID22527507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2781878..2786505hg38UCSC Ensembl
chr12:2891044..2895671hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg384628
hg194628
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469617
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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