A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997474



Internal ID19157010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:118656945..118677873hg38UCSC Ensembl
Innerchr1:119199568..119220496hg19UCSC Ensembl
Innerchr1:119001091..119022019hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3820929
hg1920929
hg1820929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv298n100
Supporting Variantsnssv3497085, nssv3488714, nssv3493591, nssv3499838, nssv3483079
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)nsv997474
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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