A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7163



Internal ID15205459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155576157..155610741hg38UCSC Ensembl
OuterchrX:154805818..154840402hg19UCSC Ensembl
OuterchrX:154459012..154493596hg18UCSC Ensembl
OuterchrX:154369522..154404106hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386405
hg196405
hg186405
hg176405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941
SamplesNA19240
Known GenesTMLHE
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)nsv7163
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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