A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008291



Internal ID19097510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105542636..105553605hg38UCSC Ensembl
Innerchr3:105261480..105272449hg19UCSC Ensembl
Innerchr3:106744170..106755139hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3810970
hg1910970
hg1810970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604388, nssv3604389
Samples
Known GenesALCAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008291
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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