A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3784



Internal ID15191825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49120027..49157254hg38UCSC Ensembl
OuterchrX:48976380..49017850hg19UCSC Ensembl
OuterchrX:48863324..48904794hg18UCSC Ensembl
OuterchrX:48732629..48774221hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3837228
hg1941471
hg1841471
hg1741593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7442
Supporting Variants
SamplesNA12878
Known GenesGPKOW
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)nssv3784
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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