A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1871



Internal ID15194469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135720375..135914069hg38UCSC Ensembl
OuterchrX:134862049..134996228hg19UCSC Ensembl
OuterchrX:134689715..134823894hg18UCSC Ensembl
OuterchrX:134587569..134721748hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38193695
hg19134180
hg18134180
hg17134180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7460
Supporting Variants
SamplesNA18555
Known GenesCT45A2, CT45A3, CT45A4, CT45A5, CT45A6, SAGE1
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)nssv1871
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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