A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019046



Internal ID19108263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141711567..141771158hg38UCSC Ensembl
Innerchr6:142032704..142092295hg19UCSC Ensembl
Innerchr6:142074397..142133988hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3859592
hg1959592
hg1859592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749554
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)nsv1019046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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