A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7175



Internal ID15552158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26597983..26686951hg38UCSC Ensembl
Outerchr1:26924474..27013442hg19UCSC Ensembl
Outerchr1:26797061..26886029hg18UCSC Ensembl
Outerchr1:26608616..26697584hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3888969
hg1988969
hg1888969
hg1788969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4025, nssv6489, nssv994, nssv6480, nssv9811, nssv5440, nssv10774, nssv5431, nssv1994
SamplesNA18507, NA12156, NA12878, NA18956, NA18555, NA19240, NA19129
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)nsv7175
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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