A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4671



Internal ID15543157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38483994..38504692hg38UCSC Ensembl
Outerchr4:38485615..38506313hg19UCSC Ensembl
Outerchr4:38162010..38182708hg18UCSC Ensembl
Outerchr4:38308181..38328879hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3820699
hg1920699
hg1820699
hg1720699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4305
Supporting Variants
SamplesNA19129
Known Genes
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)nssv4671
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