A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7404



Internal ID15552410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107378290..107463822hg38UCSC Ensembl
Outerchr7:107018735..107104267hg19UCSC Ensembl
Outerchr7:106805971..106891503hg18UCSC Ensembl
Outerchr7:106612686..106698218hg17UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3885533
hg1985533
hg1885533
hg1785533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10573, nssv6160
SamplesNA12156, NA18956
Known GenesCOG5
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)nsv7404
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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