A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9484



Internal ID15193512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55437684..55491342hg38UCSC Ensembl
OuterchrX:55464117..55517775hg19UCSC Ensembl
OuterchrX:55480842..55534500hg18UCSC Ensembl
OuterchrX:55347138..55400796hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3853659
hg1953659
hg1853659
hg1753659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7448
Supporting Variants
SamplesNA18517
Known GenesMAGEH1, MIR4536-1, USP51
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)nssv9484
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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