A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv210



Internal ID15037012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:104007896..104083797hg38UCSC Ensembl
OuterchrX:103262468..103328482hg19UCSC Ensembl
OuterchrX:103149124..103215138hg18UCSC Ensembl
OuterchrX:103068613..103134627hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3875902
hg1966015
hg1866015
hg1766015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5n1
Supporting Variantsnssv210
SamplesNA15510
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nsv210
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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