A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062581



Internal ID19151800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42488885..42554473hg38UCSC Ensembl
Innerchr22:42884891..42950479hg19UCSC Ensembl
Innerchr22:41214835..41280423hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3865589
hg1965589
hg1865589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4577n100
Supporting Variantsnssv3737355, nssv3590836, nssv3590834, nssv3737356, nssv3590827, nssv3590833, nssv3590835, nssv3737354, nssv3590832, nssv3590831, nssv3590828, nssv3590830, nssv3590829, nssv3590826
Samples
Known GenesRRP7A, SERHL, SERHL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062581
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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