A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245524



Internal ID21308638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:153701198..153720772hg38UCSC Ensembl
Outerchr1:153699771..153722864hg38UCSC Ensembl
Innerchr1:153673674..153693248hg19UCSC Ensembl
Outerchr1:153672247..153695340hg19UCSC Ensembl
Innerchr1:151940298..151959872hg18UCSC Ensembl
Outerchr1:151938871..151961964hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3823094
hg1923094
hg1823094
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170222
Supporting Variants
SamplesNGO_43
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245524
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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