A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5242



Internal ID15197148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101566380..101608895hg38UCSC Ensembl
OuterchrX:100821357..100863875hg19UCSC Ensembl
OuterchrX:100708013..100750531hg18UCSC Ensembl
OuterchrX:100627502..100670020hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3842516
hg1942519
hg1842519
hg1742519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7452
Supporting Variants
SamplesNA19129
Known Genes
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)nssv5242
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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