A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030116



Internal ID18772647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162852675..163104646hg38UCSC Ensembl
Innerchr6:163273707..163525678hg19UCSC Ensembl
Innerchr6:163193697..163445668hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38251972
hg19251972
hg18251972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749612
Samples
Known GenesPACRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030116
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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