A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018028



Internal ID19107245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80428294..80491980hg38UCSC Ensembl
Innerchr6:81138011..81201697hg19UCSC Ensembl
Innerchr6:81194730..81258416hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3863687
hg1963687
hg1863687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6071n100
Supporting Variantsnssv3648812
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)nsv1018028
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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