A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3816



Internal ID15191857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103949480..104051572hg38UCSC Ensembl
OuterchrX:103204054..103306138hg19UCSC Ensembl
OuterchrX:103090710..103192794hg18UCSC Ensembl
OuterchrX:103010199..103112283hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38102093
hg19102085
hg18102085
hg17102085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7453
Supporting Variants
SamplesNA12878
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256, TMSB15B
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)nssv3816
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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