A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11215



Internal ID15192678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49119846..49157254hg38UCSC Ensembl
OuterchrX:48976199..49017427hg19UCSC Ensembl
OuterchrX:48863143..48904371hg18UCSC Ensembl
OuterchrX:48732448..48773798hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3837409
hg1941229
hg1841229
hg1741351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7442
Supporting Variants
SamplesNA15510
Known GenesGPKOW
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)nssv11215
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