A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169450



Internal ID21313933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25219413..25232028hg38UCSC Ensembl
Outerchr7:25216626..25235278hg38UCSC Ensembl
Innerchr7:25259032..25271647hg19UCSC Ensembl
Outerchr7:25256245..25274897hg19UCSC Ensembl
Innerchr7:25225557..25238172hg18UCSC Ensembl
Outerchr7:25222770..25241422hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3818653
hg1918653
hg1818653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243144
SamplesNGO_24
Known GenesNPVF
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169450
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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