A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9765



Internal ID15540088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42604355..42649383hg38UCSC Ensembl
Outerchr9:44321736..44366764hg19UCSC Ensembl
Outerchr9:44261732..44306760hg18UCSC Ensembl
Outerchr9:43472809..43517837hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3845029
hg1945029
hg1845029
hg1745029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7423
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)nssv9765
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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