A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7115



Internal ID15552092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:138910767..138944289hg38UCSC Ensembl
OuterchrX:137992929..138026451hg19UCSC Ensembl
OuterchrX:137820595..137854117hg18UCSC Ensembl
OuterchrX:137718449..137751971hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg385905
hg195905
hg185905
hg175905
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8791
SamplesNA12156
Known GenesFGF13
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)nsv7115
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