A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033968



Internal ID19123190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60683817..61115192hg38UCSC Ensembl
Innerchr6:57651564..58082939hg19UCSC Ensembl
Innerchr6:57759523..58190898hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38431376
hg19431376
hg18431376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5971n100
Supporting Variantsnssv3745511
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)nsv1033968
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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