A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021422



Internal ID19110639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168787638..168822314hg38UCSC Ensembl
Innerchr6:169187733..169222409hg19UCSC Ensembl
Innerchr6:168929658..168964334hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3834677
hg1934677
hg1834677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6201n100
Supporting Variantsnssv3749715
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)nsv1021422
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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