A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048086



Internal ID19137305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83425985..83444817hg38UCSC Ensembl
Innerchr9:86040900..86059732hg19UCSC Ensembl
Innerchr9:85230720..85249552hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3818833
hg1918833
hg1818833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697523
Samples
Known GenesFRMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048086
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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