A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832315



Internal ID6158039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:201333591..201495116hg19UCSC Ensembl
Outerchr1:199600214..199761739hg18UCSC Ensembl
Outerchr1:198065248..198226773hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1441616
Samples
Known GenesCSRP1, LAD1, PHLDA3, RPS10P7, TNNI1, TNNT2
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832315
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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