A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9439



Internal ID15540390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54201332..54298648hg38UCSC Ensembl
Outerchr7:54269025..54366341hg19UCSC Ensembl
Outerchr7:54236519..54333835hg18UCSC Ensembl
Outerchr7:54043234..54140550hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3897317
hg1997317
hg1897317
hg1797317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7397
Supporting Variants
SamplesNA18517
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)nssv9439
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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