A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058476



Internal ID18801007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36142329..36183513hg38UCSC Ensembl
Innerchr22:36538377..36579561hg19UCSC Ensembl
Innerchr22:34868323..34909507hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3841185
hg1941185
hg1841185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4563n100
Supporting Variantsnssv3600844
Samples
Known GenesAPOL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058476
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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