A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6313



Internal ID15190865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:17405824..17411645hg38UCSC Ensembl
OuterchrX:17423947..17429768hg19UCSC Ensembl
OuterchrX:17333868..17339689hg18UCSC Ensembl
OuterchrX:17183604..17189425hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg385822
hg195822
hg185822
hg175822
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7438
Supporting Variants
SamplesNA12156
Known GenesNHS
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)nssv6313
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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