A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031334



Internal ID19120556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165144061..165209120hg38UCSC Ensembl
Innerchr6:165557550..165622609hg19UCSC Ensembl
Innerchr6:165477540..165542599hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3865060
hg1965060
hg1865060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655396
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)nsv1031334
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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