A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009830



Internal ID19099049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34768672..34828370hg38UCSC Ensembl
Innerchr4:34770294..34829992hg19UCSC Ensembl
Innerchr4:34446689..34506387hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3859699
hg1959699
hg1859699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n100
Supporting Variantsnssv3620795, nssv3620791, nssv3620801, nssv3620803, nssv3620797, nssv3620802, nssv3620798, nssv3620790, nssv3620792, nssv3620794, nssv3620800, nssv3620799, nssv3620796, nssv3620789, nssv3737786, nssv3620793, nssv3737787
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009830
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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