A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832411



Internal ID6158135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:52741587..52887864hg19UCSC Ensembl
Outerchr12:51027854..51174131hg18UCSC Ensembl
Outerchr12:51027854..51174131hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1449832, nssv1449833, nssv1449831
Samples
Known GenesKRT6A, KRT6B, KRT6C, KRT75, KRT82, KRT84, KRT85
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832411
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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