A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6645



Internal ID15537218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82880320..82889789hg38UCSC Ensembl
Outerchr15:83549072..83558541hg19UCSC Ensembl
Outerchr15:81346126..81349545hg18UCSC Ensembl
Outerchr15:81346126..81349545hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387683
hg197683
hg187683
hg177683
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1641
Supporting Variants
SamplesNA12156
Known GenesHOMER2
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)nssv6645
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