A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519446



Internal ID15100053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40626720..40632343hg38UCSC Ensembl
Innerchr8:40484239..40489862hg19UCSC Ensembl
Innerchr8:40603396..40609019hg18UCSC Ensembl
Innerchr8:40603396..40609019hg17UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385624
hg195624
hg185624
hg175624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696858
Samples
Known GenesZMAT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519446
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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