A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517204



Internal ID15444497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8724459..8726631hg38UCSC Ensembl
Innerchr18:8724457..8726629hg19UCSC Ensembl
Innerchr18:8714457..8716629hg18UCSC Ensembl
Innerchr18:8714457..8716629hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg382173
hg192173
hg182173
hg172173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656586, nssv654004, nssv669710, nssv680818
Samples
Known GenesSOGA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517204
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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