A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576545



Internal ID16363954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15047754..15108190hg38UCSC Ensembl
Innerchr18:15047753..15108189hg19UCSC Ensembl
Innerchr18:15037753..15098189hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3860437
hg1960437
hg1860437
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878463, nssv878466, nssv878464, nssv878465, nssv878467
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576545
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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