A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6938



Internal ID15536925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25773476..26120437hg38UCSC Ensembl
Outerchr20:25754112..26101073hg19UCSC Ensembl
Outerchr20:25702112..26049073hg18UCSC Ensembl
Outerchr20:25702112..26049073hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38346962
hg19346962
hg18346962
hg17346962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7340
Supporting Variants
SamplesNA12156
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)nssv6938
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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