A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9641



Internal ID15540162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49492988..49583923hg38UCSC Ensembl
Outerchr4:49495005..49585940hg19UCSC Ensembl
Outerchr4:49189762..49280697hg18UCSC Ensembl
Outerchr4:49335933..49426868hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3890936
hg1990936
hg1890936
hg1790936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7361
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)nssv9641
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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