A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11222



Internal ID15192671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:104007870..104083830hg38UCSC Ensembl
OuterchrX:103262442..103328515hg19UCSC Ensembl
OuterchrX:103149098..103215171hg18UCSC Ensembl
OuterchrX:103068587..103134660hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3875961
hg1966074
hg1866074
hg1766074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7453
Supporting Variants
SamplesNA15510
Known GenesH2BFM, H2BFWT, 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)nssv11222
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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