A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522456



Internal ID15449749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44313979..44321110hg38UCSC Ensembl
Innerchr6:44281716..44288847hg19UCSC Ensembl
Innerchr6:44389694..44396825hg18UCSC Ensembl
Innerchr6:44389694..44396825hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387132
hg197132
hg187132
hg177132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705819
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522456
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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