A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516456



Internal ID15443749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44314579..44330572hg38UCSC Ensembl
Innerchr6:44282316..44298309hg19UCSC Ensembl
Innerchr6:44390294..44406287hg18UCSC Ensembl
Innerchr6:44390294..44406287hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3815994
hg1915994
hg1815994
hg1715994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684444, nssv668519
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516456
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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