A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908825



Internal ID6270752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73987373..74022661hg19UCSC Ensembl
Outerchr17:73969953..74040293hg19UCSC Ensembl
Innerchr17:71498968..71534256hg18UCSC Ensembl
Outerchr17:71481548..71551888hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1530898, nssv1575172, nssv1586029
SamplesIS33684, IS37646, MS10311
Known GenesACOX1, C17orf106-CDK3, CDK3, EVPL, SRP68, TEN1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908825
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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