A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939



Internal ID15198373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154349311..154423689hg38UCSC Ensembl
OuterchrX:153577679..153652031hg19UCSC Ensembl
OuterchrX:153230873..153305225hg18UCSC Ensembl
OuterchrX:153098526..153172878hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3874379
hg1974353
hg1874353
hg1774353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7468
Supporting Variants
SamplesNA19240
Known GenesDNASE1L1, EMD, FLNA, RPL10, SNORA70, TAZ
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)nssv939
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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