A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530



Internal ID15538258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54202210..54302295hg38UCSC Ensembl
Outerchr7:54269903..54369988hg19UCSC Ensembl
Outerchr7:54237397..54337482hg18UCSC Ensembl
Outerchr7:54044112..54144197hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38100086
hg19100086
hg18100086
hg17100086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7397
Supporting Variants
SamplesNA12878
Known GenesHPVC1
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)nssv3530
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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