A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438167



Internal ID15041398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28278878..28281030hg38UCSC Ensembl
Innerchr10:28567807..28569959hg19UCSC Ensembl
Innerchr10:28607813..28609965hg18UCSC Ensembl
Innerchr10:28571813..28573965hg16UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg382153
hg192153
hg182153
hg162153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470267, nssv470268
SamplesNA19093, NA19094
Known GenesMPP7
MethodSNP array
AnalysisMendelian inconsistencies - for each genotype assay and population sample we defined the Mendel failure pattern of that assay as the binary vector (length 60) of Mendel consistency status across the 60 parent-offspring pair.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nsv438167
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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