A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10713



Internal ID15195399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55479980..55535227hg38UCSC Ensembl
OuterchrX:55506413..55561660hg19UCSC Ensembl
OuterchrX:55523138..55578385hg18UCSC Ensembl
OuterchrX:55389434..55444681hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3855248
hg1955248
hg1855248
hg1755248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7448
Supporting Variants
SamplesNA18956
Known GenesUSP51
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)nssv10713
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer