A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1836



Internal ID15194434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49329575..49330430hg38UCSC Ensembl
OuterchrX:49186053..49186908hg19UCSC Ensembl
OuterchrX:49072997..49073852hg18UCSC Ensembl
OuterchrX:48942424..48943279hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3834759
hg1934759
hg1834759
hg1734759
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6897
Supporting Variants
SamplesNA18555
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)nssv1836
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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