A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10703



Internal ID15195409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49121075..49157254hg38UCSC Ensembl
OuterchrX:48977428..49017906hg19UCSC Ensembl
OuterchrX:48864372..48904850hg18UCSC Ensembl
OuterchrX:48733677..48774277hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3836180
hg1940479
hg1840479
hg1740601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7442
Supporting Variants
SamplesNA18956
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)nssv10703
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