A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003368



Internal ID19092587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112383718..112395969hg38UCSC Ensembl
Innerchr3:112102565..112114816hg19UCSC Ensembl
Innerchr3:113585255..113597506hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3812252
hg1912252
hg1812252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4839n100
Supporting Variantsnssv3604432, nssv3604434, nssv3735259, nssv3604431, nssv3604433, nssv3604435, nssv3735258, nssv3604430, nssv3735257
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)nsv1003368
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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