A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455606



Internal ID22513483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7791191..7793710hg38UCSC Ensembl
chr12:7943787..7946306hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg382520
hg192520
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858089
Supporting Variants
Samples
Known GenesNANOG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455606
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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