A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7361



Internal ID15552363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49491432..49589514hg38UCSC Ensembl
Outerchr4:49493449..49591531hg19UCSC Ensembl
Outerchr4:49188206..49286288hg18UCSC Ensembl
Outerchr4:49334377..49432459hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3898083
hg1998083
hg1898083
hg1798083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9641, nssv7083, nssv11084, nssv4743, nssv387, nssv3254
SamplesNA18507, NA12156, NA12878, NA15510, NA19240, NA19129
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)nsv7361
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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