A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022985



Internal ID19112202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102993108..103152660hg38UCSC Ensembl
Innerchr6:103440983..103600535hg19UCSC Ensembl
Innerchr6:103547676..103707228hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38159553
hg19159553
hg18159553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649876
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)nsv1022985
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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