A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525725



Internal ID15106332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10112318..10112795hg38UCSC Ensembl
Innerchr16:10206175..10206652hg19UCSC Ensembl
Innerchr16:10113676..10114153hg18UCSC Ensembl
Innerchr16:10113676..10114153hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38478
hg19478
hg18478
hg17478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701889
Samples
Known GenesGRIN2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525725
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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