A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2395



Internal ID15540740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50855332..50887906hg38UCSC Ensembl
Outerchr3:50892763..50925337hg19UCSC Ensembl
Outerchr3:50867767..50904125hg18UCSC Ensembl
Outerchr3:50867767..50904125hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3832575
hg1932575
hg1836359
hg1736359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7353
Supporting Variants
SamplesNA18555
Known GenesDOCK3
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)nssv2395
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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