A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7402



Internal ID15205722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74806391..75102519hg38UCSC Ensembl
Outerchr7:74220732..74518311hg19UCSC Ensembl
Outerchr7:73858668..74156247hg18UCSC Ensembl
Outerchr7:73665383..73962962hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38296129
hg19297580
hg18297580
hg17297580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6143, nssv6145
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)nsv7402
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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