A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528833



Internal ID15456126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:78641630..78721037hg38UCSC Ensembl
Innerchr5:77937453..78016860hg19UCSC Ensembl
Innerchr5:77973209..78052616hg18UCSC Ensembl
Innerchr5:77973209..78052616hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3879408
hg1979408
hg1879408
hg1779408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705508
Samples
Known GenesLHFPL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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