A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065877



Internal ID18808408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24915337..24972338hg38UCSC Ensembl
Innerchr22:25311304..25368305hg19UCSC Ensembl
Innerchr22:23641304..23698305hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3857002
hg1957002
hg1857002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3588057
Samples
Known GenesSGSM1, TMEM211
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065877
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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