A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893



Internal ID15545145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:96046433..96065595hg38UCSC Ensembl
OuterchrX:95301432..95320594hg19UCSC Ensembl
OuterchrX:95188088..95207250hg18UCSC Ensembl
OuterchrX:95107577..95126739hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3819163
hg1919163
hg1819163
hg1719163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6997
Supporting Variants
SamplesNA19240
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)nssv893
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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