A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033784



Internal ID19123005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168787638..168818901hg38UCSC Ensembl
Innerchr6:169187733..169218996hg19UCSC Ensembl
Innerchr6:168929658..168960921hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3831264
hg1931264
hg1831264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6201n100
Supporting Variantsnssv3749714
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)nsv1033784
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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