A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv932



Internal ID15198299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149572731..149624399hg19UCSC Ensembl
OuterchrX:149323389..149375057hg18UCSC Ensembl
OuterchrX:149243299..149294967hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg1951669
hg1851669
hg1751669
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA19240
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)nssv932
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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