A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057424



Internal ID19146643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76695215..76762887hg38UCSC Ensembl
Innerchr18:74407171..74474843hg19UCSC Ensembl
Innerchr18:72536159..72603831hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3867673
hg1967673
hg1867673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n100
Supporting Variantsnssv3563034
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057424
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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