A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10710



Internal ID15195402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:52671205..52825007hg38UCSC Ensembl
OuterchrX:52700255..52854056hg19UCSC Ensembl
OuterchrX:52716980..52870781hg18UCSC Ensembl
OuterchrX:52583276..52737077hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38153803
hg19153802
hg18153802
hg17153802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7446
Supporting Variants
SamplesNA18956
Known GenesSPANXN5, SSX2, SSX2B, XAGE5
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)nssv10710
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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