A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3187



Internal ID15191229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:101557662..101562692hg38UCSC Ensembl
Outerchr3:101276506..101281536hg19UCSC Ensembl
Outerchr3:102759196..102764226hg18UCSC Ensembl
Outerchr3:102759196..102764226hg17UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg386162
hg196162
hg186162
hg176162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925
Supporting Variants
SamplesNA12878
Known GenesTRMT10C
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)nssv3187
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