A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7093



Internal ID15552068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:132609330..132636200hg38UCSC Ensembl
OuterchrX:131743358..131770228hg19UCSC Ensembl
OuterchrX:131571039..131597909hg18UCSC Ensembl
OuterchrX:131468893..131495763hg17UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg386066
hg196066
hg186066
hg176066
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8782
SamplesNA12156
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)nsv7093
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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