A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9596



Internal ID15539718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25773690..26127891hg38UCSC Ensembl
Outerchr20:25754326..26108527hg19UCSC Ensembl
Outerchr20:25702326..26056527hg18UCSC Ensembl
Outerchr20:25702326..26056527hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38354202
hg19354202
hg18354202
hg17354202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7340
Supporting Variants
SamplesNA18507
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)nssv9596
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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