A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3828



Internal ID15191869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149572070..149624889hg19UCSC Ensembl
OuterchrX:149322728..149375547hg18UCSC Ensembl
OuterchrX:149242638..149295457hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg1952820
hg1852820
hg1752820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA12878
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)nssv3828
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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