A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688



Internal ID15198615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:141902519..141943197hg38UCSC Ensembl
Outerchr7:141602319..141642997hg19UCSC Ensembl
Outerchr7:141248788..141289466hg18UCSC Ensembl
Outerchr7:141055503..141096181hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3840679
hg1940679
hg1840679
hg1740679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5974
Supporting Variants
SamplesNA19240
Known GenesCLEC5A, OR9A4
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)nssv688
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