A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10384



Internal ID15542414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187380305..187423396hg38UCSC Ensembl
Outerchr3:187098093..187141184hg19UCSC Ensembl
Outerchr3:188580787..188623878hg18UCSC Ensembl
Outerchr3:188580795..188623886hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3843092
hg1943092
hg1843092
hg1743092
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7357
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)nssv10384
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer