A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv219



Internal ID15037021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154332731..154360518hg38UCSC Ensembl
OuterchrX:153561081..153588886hg19UCSC Ensembl
OuterchrX:153214275..153242080hg18UCSC Ensembl
OuterchrX:153081928..153109733hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3827788
hg1927806
hg1827806
hg1727806
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv219
SamplesNA15510
Known GenesFLNA
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nsv219
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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