A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615981



Internal ID16056704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136640251..136725859hg38UCSC Ensembl
Innerchr9:139534703..139620311hg19UCSC Ensembl
Innerchr9:138654524..138740132hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3885609
hg1985609
hg1885609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13006n54
Supporting Variantsnssv1176164
Samples1780862100_A
Known GenesAGPAT2, EGFL7, FAM69B, MIR126, SNHG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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