A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7452



Internal ID15552463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101563740..101648990hg38UCSC Ensembl
OuterchrX:100818723..100903977hg19UCSC Ensembl
OuterchrX:100705379..100790633hg18UCSC Ensembl
OuterchrX:100624868..100710122hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3885251
hg1985255
hg1885255
hg1785255
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11219, nssv5242, nssv6357, nssv10723
SamplesNA12156, NA18956, NA15510, NA19129
Known GenesARMCX3, ARMCX6
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)nsv7452
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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