A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004215



Internal ID19093432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44522..131223hg38UCSC Ensembl
Innerchr3:86204..172906hg19UCSC Ensembl
Innerchr3:61204..147906hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3886702
hg1986703
hg1886703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4611n100
Supporting Variantsnssv3590255
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)nsv1004215
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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