A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7411



Internal ID15205732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144160778..144412427hg38UCSC Ensembl
Outerchr7:143857871..144109520hg19UCSC Ensembl
Outerchr7:143488804..143740453hg18UCSC Ensembl
Outerchr7:143295519..143547168hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38251650
hg19251650
hg18251650
hg17251650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10586, nssv3587, nssv10587, nssv1693, nssv9451, nssv10585, nssv1695, nssv6176, nssv9732, nssv3589, nssv691, nssv3588, nssv9731, nssv692, nssv5029, nssv1694, nssv6177, nssv10584, nssv9450
SamplesNA18507, NA12156, NA12878, NA18956, NA18555, NA18517, NA19240, NA19129
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, NOBOX, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
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)nsv7411
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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