A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11214



Internal ID15192679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46780291..46824570hg19UCSC Ensembl
OuterchrX:46665235..46709514hg18UCSC Ensembl
OuterchrX:46536545..46580824hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg1944280
hg1844280
hg1744280
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7440
Supporting Variants
SamplesNA15510
Known GenesJADE3
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)nssv11214
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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