A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6901



Internal ID15205171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49688138..49717812hg38UCSC Ensembl
OuterchrX:49452741..49482415hg19UCSC Ensembl
OuterchrX:49339695..49369164hg18UCSC Ensembl
OuterchrX:49155991..49185460hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg389810
hg199810
hg189810
hg179810
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5225
SamplesNA19129
Known GenesPAGE1
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)nsv6901
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