A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3127



Internal ID15540848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:44069354..44103185hg38UCSC Ensembl
Outerchr4:44071371..44105202hg19UCSC Ensembl
Outerchr4:43766128..43799959hg18UCSC Ensembl
Outerchr4:43912299..43946130hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386188
hg196188
hg186188
hg176188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4316
Supporting Variants
SamplesNA18555
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)nssv3127
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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