A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7457



Internal ID15205782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120006842..120219579hg38UCSC Ensembl
OuterchrX:119140799..119353427hg19UCSC Ensembl
OuterchrX:119024827..119237455hg18UCSC Ensembl
OuterchrX:118922681..119135309hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38212738
hg19212629
hg18212629
hg17212629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10731, nssv10729, nssv10730, nssv5256, nssv3824, nssv5257, nssv10732
SamplesNA18956, NA19129, NA12878
Known GenesRHOXF1, RHOXF2, RHOXF2B
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)nsv7457
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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