A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1879



Internal ID15194476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149533381..149583986hg19UCSC Ensembl
OuterchrX:149284039..149334644hg18UCSC Ensembl
OuterchrX:149203949..149254554hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg1950606
hg1850606
hg1750606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA18555
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)nssv1879
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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