A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022872



Internal ID19112090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:83446912..83507684hg38UCSC Ensembl
Innerchr6:84156631..84217403hg19UCSC Ensembl
Innerchr6:84213350..84274122hg18UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3860773
hg1960773
hg1860773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648889
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)nsv1022872
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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