A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7407



Internal ID15552413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:132900505..132940526hg38UCSC Ensembl
Outerchr7:132585265..132625286hg19UCSC Ensembl
Outerchr7:132235805..132275826hg18UCSC Ensembl
Outerchr7:132042520..132082541hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3840022
hg1940022
hg1840022
hg1740022
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3580
SamplesNA12878
Known GenesCHCHD3
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)nsv7407
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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