A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7101



Internal ID15190077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87890897..87934614hg38UCSC Ensembl
Outerchr4:88812049..88855766hg19UCSC Ensembl
Outerchr4:89031073..89074790hg18UCSC Ensembl
Outerchr4:89169228..89212945hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3843718
hg1943718
hg1843718
hg1743718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA12156
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)nssv7101
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