A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5232



Internal ID15543905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:73016234..73105236hg38UCSC Ensembl
OuterchrX:72236073..72325075hg19UCSC Ensembl
OuterchrX:72152798..72241800hg18UCSC Ensembl
OuterchrX:72019094..72108096hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3889003
hg1989003
hg1889003
hg1789003
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7451
Supporting Variants
SamplesNA19129
Known GenesPABPC1L2A
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)nssv5232
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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