A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10584



Internal ID15195528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144178983..144332027hg38UCSC Ensembl
Outerchr7:143876076..144029120hg19UCSC Ensembl
Outerchr7:143507009..143660053hg18UCSC Ensembl
Outerchr7:143313724..143466768hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38153045
hg19153045
hg18153045
hg17153045
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA18956
Known GenesARHGEF34P, ARHGEF35, CTAGE4, CTAGE8, 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)nssv10584
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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