A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600844



Internal ID18552439
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 StatusS
Merged Variantsnsv1058476
Supporting Variants
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)nssv3600844
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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