A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684



Internal ID15545293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131750140..131793499hg38UCSC Ensembl
Outerchr7:131434899..131478258hg19UCSC Ensembl
Outerchr7:131085439..131128798hg18UCSC Ensembl
Outerchr7:130892154..130935513hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3843360
hg1943360
hg1843360
hg1743360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7406
Supporting Variants
SamplesNA19240
Known Genes
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)nssv684
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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