A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3835



Internal ID15538562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155550486..155581248hg38UCSC Ensembl
OuterchrX:154780147..154810909hg19UCSC Ensembl
OuterchrX:154433341..154464103hg18UCSC Ensembl
OuterchrX:154343851..154374613hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3830763
hg1930763
hg1830763
hg1730763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7162
Supporting Variants
SamplesNA12878
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)nssv3835
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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