A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3811



Internal ID15538538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:96031392..96064904hg38UCSC Ensembl
OuterchrX:95286391..95319903hg19UCSC Ensembl
OuterchrX:95173047..95206559hg18UCSC Ensembl
OuterchrX:95092536..95126048hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3833513
hg1933513
hg1833513
hg1733513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6997
Supporting Variants
SamplesNA12878
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)nssv3811
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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