A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5267



Internal ID15196958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150372478..150402801hg38UCSC Ensembl
OuterchrX:149540746..149579481hg19UCSC Ensembl
OuterchrX:149291404..149330139hg18UCSC Ensembl
OuterchrX:149211314..149250049hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3830324
hg1938736
hg1838736
hg1738736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA19129
Known GenesMAMLD1
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)nssv5267
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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