A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7451



Internal ID15552462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:72972887..73105236hg38UCSC Ensembl
OuterchrX:72192722..72325075hg19UCSC Ensembl
OuterchrX:72109447..72241800hg18UCSC Ensembl
OuterchrX:71975743..72108096hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38132350
hg19132354
hg18132354
hg17132354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv885, nssv5232, nssv5231
SamplesNA19240, NA19129
Known GenesPABPC1L2A, PABPC1L2B
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)nsv7451
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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