A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017076



Internal ID19106293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164524134..164774062hg38UCSC Ensembl
Innerchr6:164945167..165195092hg19UCSC Ensembl
Innerchr6:164865157..165115082hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38249929
hg19249926
hg18249926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749616
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)nsv1017076
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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