A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3498826



Internal ID19086467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166205279..166259149hg38UCSC Ensembl
Innerchr1:166174516..166228386hg19UCSC Ensembl
Innerchr1:164441140..164495010hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3853871
hg1953871
hg1853871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998231
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)nssv3498826
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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