A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9365



Internal ID15540316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25775152..26120602hg38UCSC Ensembl
Outerchr20:25755788..26101238hg19UCSC Ensembl
Outerchr20:25703788..26049238hg18UCSC Ensembl
Outerchr20:25703788..26049238hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38345451
hg19345451
hg18345451
hg17345451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7340
Supporting Variants
SamplesNA18517
Known GenesFAM182A, FAM182B, LOC100134868, NCOR1P1
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)nssv9365
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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