A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7147



Internal ID15205441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149477626..149479012hg38UCSC Ensembl
OuterchrX:148559157..148560543hg19UCSC Ensembl
OuterchrX:148367063..148368449hg18UCSC Ensembl
OuterchrX:148264917..148266303hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386277
hg196277
hg186277
hg176277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8805
SamplesNA12156
Known GenesIDS
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)nsv7147
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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