A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7448



Internal ID15205772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55437684..55547739hg38UCSC Ensembl
OuterchrX:55464117..55574172hg19UCSC Ensembl
OuterchrX:55480842..55590897hg18UCSC Ensembl
OuterchrX:55347138..55457193hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38110056
hg19110056
hg18110056
hg17110056
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10713, nssv9484, nssv9777, nssv6335, nssv10712
SamplesNA18507, NA12156, NA18956, NA18517
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)nsv7448
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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