A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10724



Internal ID15542074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:106241559..106286573hg38UCSC Ensembl
OuterchrX:105484775..105529789hg19UCSC Ensembl
OuterchrX:105371431..105416445hg18UCSC Ensembl
OuterchrX:105290920..105335934hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3845015
hg1945015
hg1845015
hg1745015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7455
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10724
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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