A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5235



Internal ID15543886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:81838349..81858957hg38UCSC Ensembl
OuterchrX:81093848..81114456hg19UCSC Ensembl
OuterchrX:80980504..81001112hg18UCSC Ensembl
OuterchrX:80899993..80920601hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3820609
hg1920609
hg1820609
hg1720609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6975
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)nssv5235
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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