A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9711



Internal ID15540052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:54207501..54296702hg38UCSC Ensembl
Outerchr7:54275194..54364395hg19UCSC Ensembl
Outerchr7:54242688..54331889hg18UCSC Ensembl
Outerchr7:54049403..54138604hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3889202
hg1989202
hg1889202
hg1789202
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)nssv9711
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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