A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526557



Internal ID15107164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88516831..88567570hg38UCSC Ensembl
Innerchr16:88583239..88633978hg19UCSC Ensembl
Innerchr16:87110740..87161479hg18UCSC Ensembl
Innerchr16:87110740..87161479hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3850740
hg1950740
hg1850740
hg1750740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702872
Samples
Known GenesZFPM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526557
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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