A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517949



Internal ID15445242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138277441..138308224hg38UCSC Ensembl
Innerchr7:137962186..137992969hg19UCSC Ensembl
Innerchr7:137612726..137643509hg18UCSC Ensembl
Innerchr7:137419441..137450224hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3830784
hg1930784
hg1830784
hg1730784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695361
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517949
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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