A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251805



Internal ID21306578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24263272..24352617hg38UCSC Ensembl
Outerchr3:24259284..24361161hg38UCSC Ensembl
Innerchr3:24304763..24394108hg19UCSC Ensembl
Outerchr3:24300775..24402652hg19UCSC Ensembl
Innerchr3:24279767..24369112hg18UCSC Ensembl
Outerchr3:24275779..24377656hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38101878
hg19101878
hg18101878
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169645
Supporting Variants
SamplesNGO_29
Known GenesTHRB
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251805
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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