A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908826



Internal ID6270753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73997474..74022661hg19UCSC Ensembl
Outerchr17:73993640..74040293hg19UCSC Ensembl
Innerchr17:71509069..71534256hg18UCSC Ensembl
Outerchr17:71505235..71551888hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549933
SamplesMS18276
Known GenesC17orf106-CDK3, CDK3, EVPL, SRP68, TEN1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908826
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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