A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5210



Internal ID15544034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:40454689..40499475hg38UCSC Ensembl
OuterchrX:40313941..40358727hg19UCSC Ensembl
OuterchrX:40198885..40243671hg18UCSC Ensembl
OuterchrX:40070171..40114957hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3844787
hg1944787
hg1844787
hg1744787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6871
Supporting Variants
SamplesNA19129
Known Genes
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)nssv5210
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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