A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv648



Internal ID15198533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76401319..76609059hg38UCSC Ensembl
Outerchr7:76030636..76238376hg19UCSC Ensembl
Outerchr7:75868572..76076312hg18UCSC Ensembl
Outerchr7:75675287..75883027hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38207741
hg19207741
hg18207741
hg17207741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7403
Supporting Variants
SamplesNA19240
Known GenesDTX2, FDPSP2, LOC100133091, 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)nssv648
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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