A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6354



Internal ID15537509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:96047726..96068576hg38UCSC Ensembl
OuterchrX:95302725..95323575hg19UCSC Ensembl
OuterchrX:95189381..95210231hg18UCSC Ensembl
OuterchrX:95108870..95129720hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3820851
hg1920851
hg1820851
hg1720851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6997
Supporting Variants
SamplesNA12156
Known GenesMIR548AE1
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)nssv6354
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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