A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576356



Internal ID16363765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295349..5296552hg38UCSC Ensembl
Innerchr18:5295348..5296551hg19UCSC Ensembl
Innerchr18:5285348..5286551hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381204
hg191204
hg181204
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5828n54
Supporting Variantsnssv877666, nssv877663, nssv877665, nssv877661, nssv877664, nssv877662
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576356
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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