A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018305



Internal ID19107522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82508183..82558223hg38UCSC Ensembl
Innerchr6:83217900..83267940hg19UCSC Ensembl
Innerchr6:83274619..83324659hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3850041
hg1950041
hg1850041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648884
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)nsv1018305
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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