A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057139



Internal ID19146358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43935880..43979356hg38UCSC Ensembl
Innerchr18:41515845..41559321hg19UCSC Ensembl
Innerchr18:39769843..39813319hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3843477
hg1943477
hg1843477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565369
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)nsv1057139
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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