A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908219



Internal ID6270146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37880978..37913201hg19UCSC Ensembl
Outerchr17:37880265..37917633hg19UCSC Ensembl
Innerchr17:35134504..35166727hg18UCSC Ensembl
Outerchr17:35133791..35171159hg18UCSC 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 Variantsnssv1510196
SamplesSP54956
Known GenesC17orf37, ERBB2, GRB7, MIR4728
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908219
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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