A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9930



Internal ID15193331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155335399..155472412hg38UCSC Ensembl
OuterchrX:154564708..154702073hg19UCSC Ensembl
OuterchrX:154217902..154355267hg18UCSC Ensembl
OuterchrX:154128412..154265777hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38137014
hg19137366
hg18137366
hg17137366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7470
Supporting Variants
SamplesNA18507
Known GenesF8A1, F8A2, F8A3, H2AFB1, H2AFB2, H2AFB3, MIR1184-1, MIR1184-2, MIR1184-3, 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)nssv9930
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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