A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526450



Internal ID15453743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106151171..106159227hg38UCSC Ensembl
Innerchr7:105791617..105799673hg19UCSC Ensembl
Innerchr7:105578853..105586909hg18UCSC Ensembl
Innerchr7:105385568..105393624hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg388057
hg198057
hg188057
hg178057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702753
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526450
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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