A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7340



Internal ID15205654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25773476..26127891hg38UCSC Ensembl
Outerchr20:25754112..26108527hg19UCSC Ensembl
Outerchr20:25702112..26056527hg18UCSC Ensembl
Outerchr20:25702112..26056527hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38354416
hg19354416
hg18354416
hg17354416
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9365, nssv6938, nssv9596, nssv10289
SamplesNA18507, NA12156, NA18956, NA18517
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)nsv7340
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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