A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056795



Internal ID18799326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6872614..6960016hg38UCSC Ensembl
Innerchr17:6775933..6863335hg19UCSC Ensembl
Innerchr17:6716657..6804059hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3887403
hg1987403
hg1887403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3095n100
Supporting Variantsnssv3560332, nssv3560331, nssv3719161, nssv3560329, nssv3560328, nssv3560330, nssv3719160
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)nsv1056795
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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