A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469851



Internal ID19063601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2806780..2925450hg38UCSC Ensembl
Innerchr1:2723345..2842015hg19UCSC Ensembl
Innerchr1:2713205..2831875hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38118671
hg19118671
hg18118671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009684
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)nssv3469851
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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