A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10842



Internal ID15541956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2304725..2320466hg38UCSC Ensembl
Outerchr1:2236164..2251905hg19UCSC Ensembl
Outerchr1:2226024..2241765hg18UCSC Ensembl
Outerchr1:2268326..2284067hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg386497
hg196497
hg186497
hg176497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742
Supporting Variants
SamplesNA18956
Known GenesSKI
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)nssv10842
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