A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055332



Internal ID19144551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27846117..27879364hg38UCSC Ensembl
Innerchr18:25426081..25459328hg19UCSC Ensembl
Innerchr18:23680079..23713326hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3833248
hg1933248
hg1833248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564144
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)nsv1055332
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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