A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017347



Internal ID18759882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27516037..27638063hg38UCSC Ensembl
Innerchr6:27483816..27605842hg19UCSC Ensembl
Innerchr6:27591795..27713821hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38122027
hg19122027
hg18122027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5937n100
Supporting Variantsnssv3655760, nssv3655759, nssv3655761
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)nsv1017347
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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