A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515665



Internal ID15096272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4116869..4131098hg38UCSC Ensembl
Innerchr7:4156501..4170730hg19UCSC Ensembl
Innerchr7:4123027..4137256hg18UCSC Ensembl
Innerchr7:3929742..3943971hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3814230
hg1914230
hg1814230
hg1714230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664294, nssv687916
Samples
Known GenesSDK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515665
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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