A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5431



Internal ID15543343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26602719..26647039hg38UCSC Ensembl
Outerchr1:26929210..26973530hg19UCSC Ensembl
Outerchr1:26801797..26846117hg18UCSC Ensembl
Outerchr1:26613352..26657672hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3844321
hg1944321
hg1844321
hg1744321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7175
Supporting Variants
SamplesNA19129
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)nssv5431
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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