A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518070



Internal ID15098677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137849881..138124093hg38UCSC Ensembl
Innerchr7:137534627..137808839hg19UCSC Ensembl
Innerchr7:137185167..137459379hg18UCSC Ensembl
Innerchr7:136991882..137266094hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38274213
hg19274213
hg18274213
hg17274213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695484
Samples
Known GenesAKR1D1, CREB3L2, LOC100130880, MIR4468
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518070
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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