A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014026



Internal ID19103246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195557541..195715699hg38UCSC Ensembl
Innerchr3:195284382..195442570hg19UCSC Ensembl
Innerchr3:196765671..196928241hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38158159
hg19158189
hg18162571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5015n100
Supporting Variantsnssv3611401, nssv3738471, nssv3611400, nssv3611399
Samples
Known GenesAPOD, MIR570, SDHAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014026
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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