A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1884



Internal ID15194481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155346288..155534547hg38UCSC Ensembl
OuterchrX:154575597..154764208hg19UCSC Ensembl
OuterchrX:154228791..154417402hg18UCSC Ensembl
OuterchrX:154139301..154327912hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38188260
hg19188612
hg18188612
hg17188612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7470
Supporting Variants
SamplesNA18555
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)nssv1884
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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