A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169763



Internal ID21313574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159290811..159334314hg38UCSC Ensembl
Innerchr7:159083500..159127004hg19UCSC Ensembl
Innerchr7:158776261..158819765hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3843504
hg1943505
hg1847673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249428
SamplesSNI_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169763
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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