A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973



Internal ID15544899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24789827..24837235hg38UCSC Ensembl
Outerchr1:25116318..25163726hg19UCSC Ensembl
Outerchr1:24988905..25036313hg18UCSC Ensembl
Outerchr1:24861624..24909032hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3847409
hg1947409
hg1847409
hg1747409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7076
Supporting Variants
SamplesNA19240
Known GenesCLIC4
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)nssv973
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