A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10660



Internal ID15542138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42596852..42658446hg38UCSC Ensembl
Outerchr9:44312673..44374267hg19UCSC Ensembl
Outerchr9:44252669..44314263hg18UCSC Ensembl
Outerchr9:43463746..43525340hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3861595
hg1961595
hg1861595
hg1761595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7423
Supporting Variants
SamplesNA18956
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)nssv10660
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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