A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7022



Internal ID15205304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:106004040..106038102hg38UCSC Ensembl
OuterchrX:105248031..105282093hg19UCSC Ensembl
OuterchrX:105134687..105168749hg18UCSC Ensembl
OuterchrX:105054176..105088238hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg386389
hg196389
hg186389
hg176389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898
SamplesNA19240
Known GenesSERPINA7
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)nsv7022
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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