A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456901



Internal ID22514781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5548719..5552018hg38UCSC Ensembl
chr12:5657885..5661184hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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