A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957



Internal ID15538684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61204351..61251984hg38UCSC Ensembl
Outerchr11:60971823..61019456hg19UCSC Ensembl
Outerchr11:60728399..60776032hg18UCSC Ensembl
Outerchr11:60728399..60776032hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3847634
hg1947634
hg1847634
hg1747634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv339
Supporting Variants
SamplesNA12878
Known GenesPGA3, PGA4, PGA5
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3957
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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