A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2912



Internal ID15541644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110936447..110970784hg38UCSC Ensembl
Outerchr13:111588794..111623131hg19UCSC Ensembl
Outerchr13:110386795..110421132hg18UCSC Ensembl
Outerchr13:110386795..110421132hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385693
hg195693
hg185693
hg175693
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1183
Supporting Variants
SamplesNA18555
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)nssv2912
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