A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9234



Internal ID15187944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:95786150..95831237hg38UCSC Ensembl
Outerchr14:96252487..96297574hg19UCSC Ensembl
Outerchr14:95322240..95367327hg18UCSC Ensembl
Outerchr14:95322240..95367327hg17UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3845088
hg1945088
hg1845088
hg1745088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1413
Supporting Variants
SamplesNA12156
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)nssv9234
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