A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7676



Internal ID15536188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34738018..34771750hg38UCSC Ensembl
Outerchr20:33325822..33359553hg19UCSC Ensembl
Outerchr20:32789483..32823214hg18UCSC Ensembl
Outerchr20:32789483..32823214hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg385708
hg195708
hg185708
hg175708
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3361
Supporting Variants
SamplesNA12156
Known GenesNCOA6
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)nssv7676
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