A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6357



Internal ID15190821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101565677..101610558hg38UCSC Ensembl
OuterchrX:100820658..100865538hg19UCSC Ensembl
OuterchrX:100707314..100752194hg18UCSC Ensembl
OuterchrX:100626803..100671683hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3844882
hg1944881
hg1844881
hg1744881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7452
Supporting Variants
SamplesNA12156
Known Genes
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)nssv6357
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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