A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7449



Internal ID15205773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:71684267..71835832hg38UCSC Ensembl
OuterchrX:70904117..71055682hg19UCSC Ensembl
OuterchrX:70820842..70972407hg18UCSC Ensembl
OuterchrX:70687138..70838703hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38151566
hg19151566
hg18151566
hg17151566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3798
SamplesNA12878
Known GenesBCYRN1, CXorf49, CXorf49B, LINC00891, LOC100132741
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)nsv7449
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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