A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2646



Internal ID15540464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:47614509..47654872hg38UCSC Ensembl
Outerchr7:47654107..47694470hg19UCSC Ensembl
Outerchr7:47620632..47660995hg18UCSC Ensembl
Outerchr7:47427347..47467710hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3840364
hg1940364
hg1840364
hg1740364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7395
Supporting Variants
SamplesNA18555
Known GenesLOC101929086
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)nssv2646
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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