A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026012



Internal ID19115229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109530435..109678176hg38UCSC Ensembl
Innerchr6:109851638..109999379hg19UCSC Ensembl
Innerchr6:109958331..110106072hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38147742
hg19147742
hg18147742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654286
Samples
Known GenesAK9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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