A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7095



Internal ID15552070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:132894999..132926335hg38UCSC Ensembl
OuterchrX:132029027..132060363hg19UCSC Ensembl
OuterchrX:131856708..131888044hg18UCSC Ensembl
OuterchrX:131754562..131785898hg17UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg389662
hg199662
hg189662
hg179662
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911
SamplesNA19240
Known GenesHS6ST2
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)nsv7095
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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