A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066453



Internal ID19155672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42376596..42488991hg38UCSC Ensembl
Innerchr22:42772602..42884997hg19UCSC Ensembl
Innerchr22:41102546..41214941hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38112396
hg19112396
hg18112396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590816
Samples
Known GenesNFAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066453
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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