A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005542



Internal ID19094759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114585306..114705318hg38UCSC Ensembl
Innerchr3:114304153..114424165hg19UCSC Ensembl
Innerchr3:115786843..115906855hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38120013
hg19120013
hg18120013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604466
Samples
Known GenesZBTB20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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