A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580



Internal ID15538308
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 Flag1
Merged StatusS
Merged Variantsnsv7407
Supporting Variants
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)nssv3580
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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