A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027441



Internal ID19116660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66932755..66954719hg38UCSC Ensembl
Innerchr6:67642648..67664612hg19UCSC Ensembl
Innerchr6:67699369..67721333hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3821965
hg1921965
hg1821965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658759
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)nsv1027441
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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