A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600795



Internal ID16041518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666535..667756hg38UCSC Ensembl
Innerchr6:666535..667756hg19UCSC Ensembl
Innerchr6:611535..612756hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381222
hg191222
hg181222
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10268n54
Supporting Variantsnssv1048511, nssv1048510
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600795
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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