A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576626



Internal ID16364035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30273518..30341970hg38UCSC Ensembl
Innerchr18:27853483..27921936hg19UCSC Ensembl
Innerchr18:26107481..26175934hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3868453
hg1968454
hg1868454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878936
Samples
Known GenesMIR302F
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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