A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576357



Internal ID16363766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5295349..5326222hg38UCSC Ensembl
Innerchr18:5295348..5326221hg19UCSC Ensembl
Innerchr18:5285348..5316221hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3830874
hg1930874
hg1830874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877668, nssv877667
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576357
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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