A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4606



Internal ID15543377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111830182..111874580hg38UCSC Ensembl
Outerchr6:112151385..112195783hg19UCSC Ensembl
Outerchr6:112258078..112302476hg18UCSC Ensembl
Outerchr6:112258078..112302476hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3844399
hg1944399
hg1844399
hg1744399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445
Supporting Variants
SamplesNA19129
Known GenesFYN
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)nssv4606
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