A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8446



Internal ID15188732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:151431931..151465556hg38UCSC Ensembl
Outerchr7:151129017..151162642hg19UCSC Ensembl
Outerchr7:150759950..150793575hg18UCSC Ensembl
Outerchr7:150566665..150600290hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg385810
hg195810
hg185810
hg175810
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006
Supporting Variants
SamplesNA12156
Known GenesCRYGN, MIR3907
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)nssv8446
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer