A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737485



Internal ID19035766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47327571..47345696hg38UCSC Ensembl
Innerchr22:47723321..47741446hg19UCSC Ensembl
Innerchr22:46101985..46120110hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3818126
hg1918126
hg1818126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057013
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3737485
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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