A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6145



Internal ID15191033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74880064..75101012hg38UCSC Ensembl
Outerchr7:74296166..74516803hg19UCSC Ensembl
Outerchr7:73934102..74154739hg18UCSC Ensembl
Outerchr7:73740817..73961454hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38220949
hg19220638
hg18220638
hg17220638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7402
Supporting Variants
SamplesNA12156
Known GenesGTF2IRD2, GTF2IRD2B, PMS2P5, STAG3L2, WBSCR16
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)nssv6145
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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