A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908214



Internal ID6270141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37815749..37856118hg19UCSC Ensembl
Outerchr17:37814224..37861833hg19UCSC Ensembl
Innerchr17:35069275..35109644hg18UCSC Ensembl
Outerchr17:35067750..35115359hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510195
SamplesSP54956
Known GenesERBB2, PGAP3, PNMT, STARD3, TCAP
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908214
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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