A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066556



Internal ID18809087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6872614..6962694hg38UCSC Ensembl
Innerchr17:6775933..6866013hg19UCSC Ensembl
Innerchr17:6716657..6806737hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3890081
hg1990081
hg1890081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3095n100
Supporting Variantsnssv3719163, nssv3560333, nssv3719162, nssv3560334
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066556
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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