A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055873



Internal ID19145092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59501461..59544227hg38UCSC Ensembl
Innerchr18:57168693..57211459hg19UCSC Ensembl
Innerchr18:55319673..55362439hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3842767
hg1942767
hg1842767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565492
Samples
Known GenesCCBE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055873
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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