A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486063



Internal ID19073704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104402443..104485887hg38UCSC Ensembl
Innerchr1:104945065..105028509hg19UCSC Ensembl
Innerchr1:104746588..104830032hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3883445
hg1983445
hg1883445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009719
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)nssv3486063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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