A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11142



Internal ID15539437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:48859346..48952199hg38UCSC Ensembl
Outerchr7:48898942..48991795hg19UCSC Ensembl
Outerchr7:48869488..48962341hg18UCSC Ensembl
Outerchr7:48676203..48769056hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3892854
hg1992854
hg1892854
hg1792854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7396
Supporting Variants
SamplesNA15510
Known GenesCDC14C
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)nssv11142
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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