A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058948



Internal ID19148167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75046878..75109329hg38UCSC Ensembl
Innerchr18:72758834..72821285hg19UCSC Ensembl
Innerchr18:70887822..70950273hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3862452
hg1962452
hg1862452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563026
Samples
Known GenesZNF407
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058948
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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