A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11220



Internal ID15192673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103950066..104049835hg38UCSC Ensembl
OuterchrX:103204640..103304403hg19UCSC Ensembl
OuterchrX:103091296..103191059hg18UCSC Ensembl
OuterchrX:103010785..103110548hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3899770
hg1999764
hg1899764
hg1799764
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7453
Supporting Variants
SamplesNA15510
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)nssv11220
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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