A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251366



Internal ID21312508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77745927..77749571hg38UCSC Ensembl
Outerchr2:77738395..77749572hg38UCSC Ensembl
Innerchr2:77973053..77976697hg19UCSC Ensembl
Outerchr2:77965521..77976698hg19UCSC Ensembl
Innerchr2:77826561..77830205hg18UCSC Ensembl
Outerchr2:77819029..77830206hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3811178
hg1911178
hg1811178
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169944
Supporting Variants
SamplesSNI_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251366
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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