A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10712



Internal ID15195400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55442032..55490474hg38UCSC Ensembl
OuterchrX:55468465..55516907hg19UCSC Ensembl
OuterchrX:55485190..55533632hg18UCSC Ensembl
OuterchrX:55351486..55399928hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3848443
hg1948443
hg1848443
hg1748443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7448
Supporting Variants
SamplesNA18956
Known GenesMAGEH1, MIR4536-1, USP51
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)nssv10712
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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