A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11219



Internal ID15192674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101607273..101648990hg38UCSC Ensembl
OuterchrX:100862253..100903977hg19UCSC Ensembl
OuterchrX:100748909..100790633hg18UCSC Ensembl
OuterchrX:100668398..100710122hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3841718
hg1941725
hg1841725
hg1741725
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7452
Supporting Variants
SamplesNA15510
Known GenesARMCX3, ARMCX6
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)nssv11219
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