A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2438



Internal ID15540693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187420484..187461822hg38UCSC Ensembl
Outerchr3:187138272..187179610hg19UCSC Ensembl
Outerchr3:188620966..188662304hg18UCSC Ensembl
Outerchr3:188620974..188662312hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3841339
hg1941339
hg1841339
hg1741339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7357
Supporting Variants
SamplesNA18555
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)nssv2438
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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