A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7403



Internal ID15205723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76401319..76659954hg38UCSC Ensembl
Outerchr7:76030636..76289271hg19UCSC Ensembl
Outerchr7:75868572..76127207hg18UCSC Ensembl
Outerchr7:75675287..75933922hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38258636
hg19258636
hg18258636
hg17258636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6146, nssv648, nssv4994
SamplesNA12156, NA19240, NA19129
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, SRCRB4D, UPK3B, ZP3
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)nsv7403
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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