A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6146



Internal ID15191032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76434026..76659954hg38UCSC Ensembl
Outerchr7:76063343..76289271hg19UCSC Ensembl
Outerchr7:75901279..76127207hg18UCSC Ensembl
Outerchr7:75707994..75933922hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38225929
hg19225929
hg18225929
hg17225929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7403
Supporting Variants
SamplesNA12156
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, 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)nssv6146
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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