A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576361



Internal ID16363770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295482..5296552hg38UCSC Ensembl
Innerchr18:5295481..5296551hg19UCSC Ensembl
Innerchr18:5285481..5286551hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381071
hg191071
hg181071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5829n54
Supporting Variantsnssv877674
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576361
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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