A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7439



Internal ID15552448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:45648559..45730667hg38UCSC Ensembl
OuterchrX:45507804..45590156hg19UCSC Ensembl
OuterchrX:45392748..45475100hg18UCSC Ensembl
OuterchrX:45264058..45346410hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3882109
hg1982353
hg1882353
hg1782353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3778, nssv10699
SamplesNA12878, NA18956
Known Genes
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)nsv7439
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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