A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518377



Internal ID15445670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3899423..3938710hg38UCSC Ensembl
Innerchr7:3939055..3978342hg19UCSC Ensembl
Innerchr7:3905581..3944868hg18UCSC Ensembl
Innerchr7:3712296..3751583hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3839288
hg1939288
hg1839288
hg1739288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695805
Samples
Known GenesSDK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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