A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009236



Internal ID19098454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186745387..186762432hg38UCSC Ensembl
Innerchr3:186463176..186480221hg19UCSC Ensembl
Innerchr3:187945870..187962915hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3817046
hg1917046
hg1817046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615033
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)nsv1009236
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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