A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669544



Internal ID15059510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:817186..833068hg38UCSC Ensembl
Innerchr1:752566..768448hg19UCSC Ensembl
Innerchr1:742429..758311hg18UCSC Ensembl
Innerchr1:792429..808311hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3815883
hg1915883
hg1815883
hg1715883
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517709
Supporting Variants
Samples
Known GenesFAM87B, LINC00115, LINC01128
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669544
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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