A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5277



Internal ID15543568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155550353..155591711hg38UCSC Ensembl
OuterchrX:154780014..154821372hg19UCSC Ensembl
OuterchrX:154433208..154474566hg18UCSC Ensembl
OuterchrX:154343718..154385076hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3841359
hg1941359
hg1841359
hg1741359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7162
Supporting Variants
SamplesNA19129
Known GenesTMLHE
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)nssv5277
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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