A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4763



Internal ID15196514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87929269..87972140hg38UCSC Ensembl
Outerchr4:88850421..88893292hg19UCSC Ensembl
Outerchr4:89069445..89112316hg18UCSC Ensembl
Outerchr4:89207600..89250471hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3842872
hg1942872
hg1842872
hg1742872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA19129
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)nssv4763
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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