A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908207



Internal ID6270134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37770005..37871745hg19UCSC Ensembl
Outerchr17:37709422..37922259hg19UCSC Ensembl
Innerchr17:35023531..35125271hg18UCSC Ensembl
Outerchr17:34962948..35175785hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1575169, nssv1586019
SamplesIS33684, IS37646
Known GenesC17orf37, ERBB2, GRB7, IKZF3, MIR4728, NEUROD2, PGAP3, PNMT, PPP1R1B, STARD3, TCAP
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908207
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer