A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6850



Internal ID15551801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:32104890..32113015hg38UCSC Ensembl
OuterchrX:32123007..32131132hg19UCSC Ensembl
OuterchrX:32032928..32041053hg18UCSC Ensembl
OuterchrX:31882664..31890789hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg386344
hg196344
hg186344
hg176344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3775
SamplesNA12878
Known GenesDMD
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)nsv6850
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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