A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907620



Internal ID6269547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4796286..5042894hg19UCSC Ensembl
Outerchr17:4778487..5048405hg19UCSC Ensembl
Innerchr17:4737062..4983618hg18UCSC Ensembl
Outerchr17:4724664..4989129hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1573932
SamplesIS33504
Known GenesC17orf107, CAMTA2, CHRNE, ENO3, GP1BA, GPR172B, INCA1, KIF1C, MINK1, PFN1, RNF167, SLC25A11, SPAG7, USP6, ZFP3, ZNF232
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907620
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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