A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531



Internal ID15538259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54249535..54332641hg38UCSC Ensembl
Outerchr7:54317228..54400334hg19UCSC Ensembl
Outerchr7:54284722..54367828hg18UCSC Ensembl
Outerchr7:54091437..54174543hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3883107
hg1983107
hg1883107
hg1783107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7397
Supporting Variants
SamplesNA12878
Known Genes
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)nssv3531
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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