A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590837



Internal ID18889118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42488885..42559770hg38UCSC Ensembl
Innerchr22:42884891..42955776hg19UCSC Ensembl
Innerchr22:41214835..41285720hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3870886
hg1970886
hg1870886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058984
Supporting Variants
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)nssv3590837
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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