A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5264



Internal ID15196978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:141105517..141445205hg38UCSC Ensembl
OuterchrX:140199691..140533199hg19UCSC Ensembl
OuterchrX:140027357..140360865hg18UCSC Ensembl
OuterchrX:139925211..140258719hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38339689
hg19333509
hg18333509
hg17333509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7462
Supporting Variants
SamplesNA19129
Known GenesLDOC1, SPANXC
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)nssv5264
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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