A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433



Internal ID15549142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:93671735..93683652hg38UCSC Ensembl
Outerchr4:94592886..94604803hg19UCSC Ensembl
Outerchr4:94811909..94823826hg18UCSC Ensembl
Outerchr4:94950064..94961981hg17UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3811918
hg1911918
hg1811918
hg1711918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4767
SamplesNA19129
Known GenesGRID2
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)nsv4433
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