A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576556



Internal ID16363965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15382822..15410817hg38UCSC Ensembl
Innerchr18:15382821..15410816hg19UCSC Ensembl
Innerchr18:15372821..15400816hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3827996
hg1927996
hg1827996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5870n54
Supporting Variantsnssv878480, nssv878481
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576556
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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