A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7156



Internal ID15205451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151673748..151705977hg38UCSC Ensembl
OuterchrX:150842220..150874449hg19UCSC Ensembl
OuterchrX:150592876..150625105hg18UCSC Ensembl
OuterchrX:150512788..150545017hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387262
hg197262
hg187262
hg177262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10745
SamplesNA18956
Known GenesPASD1, PRRG3
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)nsv7156
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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