A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243727



Internal ID21306437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76696440..76920885hg38UCSC Ensembl
Outerchr7:76681343..76927895hg38UCSC Ensembl
Innerchr7:76325757..76550202hg19UCSC Ensembl
Outerchr7:76310660..76557212hg19UCSC Ensembl
Innerchr7:76163693..76388138hg18UCSC Ensembl
Outerchr7:76148596..76395148hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38246553
hg19246553
hg18246553
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170160
Supporting Variants
SamplesNGO_28
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243727
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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