A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8032



Internal ID15189146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:173295875..173323425hg38UCSC Ensembl
Outerchr4:174217026..174244576hg19UCSC Ensembl
Outerchr4:174453601..174481151hg18UCSC Ensembl
Outerchr4:174591756..174619306hg17UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3827551
hg1927551
hg1827551
hg1727551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4610
Supporting Variants
SamplesNA12156
Known GenesGALNT7
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)nssv8032
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