A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737417



Internal ID18689012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42501264..42577195hg38UCSC Ensembl
Innerchr22:42897270..42973201hg19UCSC Ensembl
Innerchr22:41227214..41303145hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3875932
hg1975932
hg1875932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065275
Supporting Variants
Samples
Known GenesRRP7A, RRP7B, 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)nssv3737417
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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