A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8711



Internal ID15535153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40855512..40889361hg38UCSC Ensembl
OuterchrX:40714765..40748614hg19UCSC Ensembl
OuterchrX:40599709..40633558hg18UCSC Ensembl
OuterchrX:40471019..40504868hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg385590
hg195590
hg185590
hg175590
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6872
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8711
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