A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2542



Internal ID15193893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:152290870..152311138hg38UCSC Ensembl
Outerchr1:152263346..152283614hg19UCSC Ensembl
Outerchr1:150529970..150550238hg18UCSC Ensembl
Outerchr1:149076419..149096687hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3820269
hg1920269
hg1820269
hg1720269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7183
Supporting Variants
SamplesNA18555
Known GenesFLG
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)nssv2542
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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