A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062925



Internal ID19152144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51202320..51235832hg38UCSC Ensembl
Innerchr18:48728690..48762202hg19UCSC Ensembl
Innerchr18:46982688..47016200hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3833513
hg1933513
hg1833513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3356n100
Supporting Variantsnssv3565445
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)nsv1062925
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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