A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv931



Internal ID15198294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150366978..150402801hg38UCSC Ensembl
OuterchrX:149535245..149580929hg19UCSC Ensembl
OuterchrX:149285903..149331587hg18UCSC Ensembl
OuterchrX:149205813..149251497hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3835824
hg1945685
hg1845685
hg1745685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7466
Supporting Variants
SamplesNA19240
Known GenesMAMLD1
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)nssv931
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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