A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10744



Internal ID15195368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150369465..150402801hg38UCSC Ensembl
OuterchrX:149537732..149577541hg19UCSC Ensembl
OuterchrX:149288390..149328199hg18UCSC Ensembl
OuterchrX:149208300..149248109hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3833337
hg1939810
hg1839810
hg1739810
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA18956
Known GenesMAMLD1
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)nssv10744
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