A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9712



Internal ID15540043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54235041..54342749hg38UCSC Ensembl
Outerchr7:54302734..54410442hg19UCSC Ensembl
Outerchr7:54270228..54377936hg18UCSC Ensembl
Outerchr7:54076943..54184651hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38107709
hg19107709
hg18107709
hg17107709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7397
Supporting Variants
SamplesNA18507
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)nssv9712
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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