A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034219



Internal ID19123441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91705167..92010209hg38UCSC Ensembl
Innerchr6:92414885..92719927hg19UCSC Ensembl
Innerchr6:92471606..92776648hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38305043
hg19305043
hg18305043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648965
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)nsv1034219
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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