A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517557



Internal ID15098164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27388748..27389146hg38UCSC Ensembl
Innerchr6:27356527..27356925hg19UCSC Ensembl
Innerchr6:27464506..27464904hg18UCSC Ensembl
Innerchr6:27464506..27464904hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38399
hg19399
hg18399
hg17399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672642, nssv652352
Samples
Known GenesZNF391
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517557
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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