A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6177



Internal ID15191001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144254512..144354426hg38UCSC Ensembl
Outerchr7:143951605..144051519hg19UCSC Ensembl
Outerchr7:143582538..143682452hg18UCSC Ensembl
Outerchr7:143389253..143489167hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3899915
hg1999915
hg1899915
hg1799915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA12156
Known GenesARHGEF34P, 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)nssv6177
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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