A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697824



Internal ID15434476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25347793..25352882hg38UCSC Ensembl
Innerchr18:22927757..22932846hg19UCSC Ensembl
Innerchr18:21181755..21186844hg18UCSC Ensembl
Innerchr18:21181755..21186844hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg385090
hg195090
hg185090
hg175090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521168
Supporting Variants
Samples
Known GenesZNF521
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697824
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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