A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6876



Internal ID15536987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:138248423..138289983hg38UCSC Ensembl
Outerchr2:139005993..139047553hg19UCSC Ensembl
Outerchr2:138722463..138764023hg18UCSC Ensembl
Outerchr2:138839725..138881285hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3841561
hg1941561
hg1841561
hg1741561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7330
Supporting Variants
SamplesNA12156
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)nssv6876
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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