A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9445



Internal ID15540396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:109789995..109832984hg38UCSC Ensembl
Outerchr7:109430052..109473041hg19UCSC Ensembl
Outerchr7:109217288..109260277hg18UCSC Ensembl
Outerchr7:109024003..109066992hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3842990
hg1942990
hg1842990
hg1742990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5896
Supporting Variants
SamplesNA18517
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)nssv9445
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