A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5220



Internal ID15544002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:48397906..48434604hg38UCSC Ensembl
OuterchrX:48257348..48292983hg19UCSC Ensembl
OuterchrX:48142292..48177927hg18UCSC Ensembl
OuterchrX:48013602..48049237hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3836699
hg1935636
hg1835636
hg1735636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7441
Supporting Variants
SamplesNA19129
Known GenesSSX4, SSX4B
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)nssv5220
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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