A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034359



Internal ID19123581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166946155..166971226hg38UCSC Ensembl
Innerchr6:167359643..167384714hg19UCSC Ensembl
Innerchr6:167279633..167304704hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3825072
hg1925072
hg1825072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749620
Samples
Known GenesRNASET2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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