A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3827



Internal ID15191868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150371178..150402801hg38UCSC Ensembl
OuterchrX:149539446..149580775hg19UCSC Ensembl
OuterchrX:149290104..149331433hg18UCSC Ensembl
OuterchrX:149210014..149251343hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3831624
hg1941330
hg1841330
hg1741330
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA12878
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)nssv3827
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