A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029624



Internal ID19118842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61114361..61350771hg38UCSC Ensembl
Innerchr6:61886428..62123350hg19UCSC Ensembl
Innerchr6:61944387..62181309hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38236411
hg19236923
hg18236923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5984n100
Supporting Variantsnssv3657583, nssv3745522, nssv3657582, nssv3745521, nssv3657584, nssv3657585, nssv3745520, nssv3657586
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)nsv1029624
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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