A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7380



Internal ID15552384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:51561613..51601699hg38UCSC Ensembl
Outerchr6:51426411..51466497hg19UCSC Ensembl
Outerchr6:51534370..51574456hg18UCSC Ensembl
Outerchr6:51534370..51574456hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3840087
hg1940087
hg1840087
hg1740087
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2590
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)nsv7380
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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