A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003336



Internal ID19092555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103226498..103244137hg38UCSC Ensembl
Innerchr3:102945342..102962981hg19UCSC Ensembl
Innerchr3:104428032..104445671hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3817640
hg1917640
hg1817640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604377
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)nsv1003336
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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