A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516517



Internal ID15443810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:96746568..96761378hg38UCSC Ensembl
Innerchr6:97194444..97209254hg19UCSC Ensembl
Innerchr6:97301165..97315975hg18UCSC Ensembl
Innerchr6:97301165..97315975hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3814811
hg1914811
hg1814811
hg1714811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690693, nssv668795, nssv680131
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516517
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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