A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1854



Internal ID15194452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:104015259..104062295hg38UCSC Ensembl
OuterchrX:103269831..103316859hg19UCSC Ensembl
OuterchrX:103156487..103203515hg18UCSC Ensembl
OuterchrX:103075976..103123004hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3847037
hg1947029
hg1847029
hg1747029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7453
Supporting Variants
SamplesNA18555
Known GenesH2BFM, H2BFXP, MIR1256
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)nssv1854
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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