A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10749



Internal ID15195363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155354436..155525235hg38UCSC Ensembl
OuterchrX:154583750..154754896hg19UCSC Ensembl
OuterchrX:154236944..154408090hg18UCSC Ensembl
OuterchrX:154147454..154318600hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38170800
hg19171147
hg18171147
hg17171147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7470
Supporting Variants
SamplesNA18956
Known GenesF8A1, F8A2, F8A3, H2AFB1, H2AFB2, H2AFB3, MIR1184-1, MIR1184-2, MIR1184-3, TMLHE, TMLHE-AS1
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)nssv10749
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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